Ex Parte 7,542,878 B2 et alDownload PDFPatent Trial and Appeal BoardDec 22, 201690010751 (P.T.A.B. Dec. 22, 2016) Copy Citation United States Patent and Trademark Office UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O.Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 90/010,751 11/30/2009 7,542,878 B2 14645-4 3683 757 7590 BGL P.O. BOX 10395 CHICAGO, IL 60610 12/22/2016 EXAMINER NASSER, ROBERT L ART UNIT PAPER NUMBER 3992 MAIL DATE DELIVERY MODE 12/22/2016 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES Ex parte CARD GUARD SCIENTIFIC SURVIVAL LTD. Appellant Appeal 2016-005923 Application 12/706,541 Reexamination Control 90/010,7511 U.S. Patent No. 7,542,878 B2 Technology Center 3900 Before RICHARD M. LEBOVITZ, MICHAEL R. ZECHER, and JENNIFER S. BISK, Administrative Patent Judges. LEBOVITZ, Administrative Patent Judge. DECISION ON APPEAL This is a decision on appeal by the Patent Owner from the Patent Examiner’s decision to finally reject claims 1, 31, 34, 36, and 37 in the above- identified ex parte reexamination of U.S. Patent No. 7,542,878 (hereinafter, 1 According to the Appeal Brief, the real party in interest is Card Guard Scientific Survival Ltd., now known as LifeWatch Technologies Ltd., which is 100% owned by LifeWatch AG. App. Br. 2. Page 2 of the Appeal Brief provides additional disclosures about the ownership and relationships between shareholders of the companies. Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 “the ’878 patent”). The Board’s jurisdiction for this appeal is under 35 U.S.C. §§ 6(b) and 134. We affirm. STATEMENT OF CASE An appeal to the Board of Patent Appeals and Interferences (now, the Patent Trial and Appeal Board) from an Examiner’s final rejection in a merged reissue and ex parte reexamination the ’878 patent was decided January 22, 2013. Decision in Appeal No. 2012-010812 (hereinafter, “the 10812 Decision”). The Examiner’s decision was affirmed-in-part. 10812 Decision 1. Subsequently, in an interview with the Examiner, Patent Owner proposed an amendment to the claims, including new claims 31—37. Patent Owner Remarks, Feb. 19, 2014. The Examiner entered the amendment and re-opened prosecution, rejecting all the pending claims. Non-final Office Action of Oct. 21, 2014. Subsequently, all claims were canceled, except for claims 1 and 31—37, and various prior art rejections were set forth by the Examiner. Non-final Office Action of Jan. 16, 2015. The Examiner denied the claims the benefit of the earlier filed Application No. 09/261,136 (“the ’136 Application”, filed Mar. 3, 1999) (now U.S. Pat. No, 6,366,871 B1 (“the ’871 patent”))2 and accorded the claims the filing date of Jun. 23, 2004. Non-final Office Action of Jan. 16, 2015, pp. 5—6. The denial of the benefit of the ’136 Application filing date was based on the determination that the ’136 Application does not describe a “multi-purpose personal data accessary,” a requirement of all the pending claims. 2 All references to the written description of the ’136 Application are with respect to the published ’871 patent. 2 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 The Examiner finally rejected all pending claims over various combinations of prior art. Final Rejection of Aug. 13,2015. Patent Owner filed a Notice of Appeal on Nov. 13, 2015 from the Examiner’s Final Rejection. Claims 32, 33, and 35 were cancelled. Claims 1,31, 34, 36, and 37 are all the pending claims. Appeal Br. 7 (Feb. 16, 2016). In the Appeal Brief, Patent Owner argues that claims 1, 31, 34, 36, and 37 are entitled to the benefit of the ’136 Application filed March 3, 1999. Appeal Br. 22. Patent Owner stated “[ejach reference cited by the Examiner, but for Davis and Rohde, has an effective prior art date after March 3, 1999. Therefore, none of the cited art, but for Davis and Rohde, can be applied against the present claims.” Id. Patent Owner further stated that “the Board previously concluded that neither Davis nor Rohde disclosed all the features of the present claims.” Id. Because Patent Owner did not provide additional arguments as to why the rejected claims are patentable over the cited prior art publications, all pending rejections turn on the question of whether claims 1, 31, 34, 36, and 37 are entitled to the benefit of the filing date of the ’136 Application. As explained in detail below, we agree with the Examiner’s decision to deny claims 1, 31, 34, 36, and 37 the benefit of the filing date of the ’136 Application. Because the benefit of the filing date is denied, all prior art rejections of claims 1, 31, 34, 36, and 37 are affirmed. The prior art rejections are listed in the Final Rejection mailed Aug. 3, 2015. Claim 1, which is representative of the appeal claims, is reproduced below: 1. A personal health monitor comprising: a physiological data input device operative to gather physiological data; and a multi purpose personal data accessory, whereas the multi-purpose personal data accessory is adapted to execute health monitoring 3 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 software such as to enable the multi-purpose personal data accessory to receive the physiological data, process the physiological data to provide processed physiological data and control a long range transmission of the processed physiological data to a remote entity. Independent claims 31, 34, 36, and 37 each require a multi-purpose personal data accessory. Consequently, the issue to be resolved in this Appeal is the same for all the rejected claims, namely, does the ’136 Application describe the claimed “multi-purpose personal data accessory”? An oral hearing was held on November 28, 2012. A transcript will be entered into the record in due course. Claim 1 is directed to a “person health monitor” comprising (1) “a physiological data input device” and (2) “a multi-purpose personal data accessory.” In the 010812 Decision, the term “multi-purpose personal data accessory” was interpreted as follows: ... to be a device which is adapted to execute the claimed health monitoring function using hardware, such as a processor, and which is not solely devoted to performing the heath monitoring function. That is, the multi-purpose personal data accessory is not “dedicated” to a single purpose or function, but has a function other than health monitoring, such as a function conventionally available on a cellular phone or palm computer. 010812 Decision 7. We adopt this definition for the purpose of this Appeal. The Examiner determined that claims 1, 31, 34, 36, and 37 were not entitled to the priority date of the ’136 Application because the Application does not describe “a multi-purpose personal data accessory.” 4 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 Patent Owner seeks to establish that the “ambulatory patient monitoring apparatus” described in ’136 Application is a “multi-purpose personal data accessory” because it is not dedicated to a single purpose or function, “but has a function other than health monitoring, such as a function conventionally available on a cellular phone or palm computer.” Appeal Br. 7. To demonstrate that the ’136 Application describes a health monitor with an additional and non-health-related function, Patent Owner provided a declaration by Harry Bims, Ph.D. (“Bims 1 Decl.” dated Nov. 13, 2015). Dr. Bims stated that he has considerable educational and work experience in wireless communications. Id., 4—8. Based on his summary of his education and work experience, we find that Dr. Bims is qualified to testify on the matters discussed in his declaration. Dr. Bims testified in this declaration that the “function other than health monitoring” is that of a cellular phone “that had the functional capability to place telephone calls to (and receive telephone calls from) other cellular devices and landline phones through the public telephone network.” Bims 1 Decl. 136. Dr. Bims testified that the person of ordinary skill in the art, who he refers to as the acronym “POSA,” would have “understood that cellular monitor 12 could be used for making and/or receiving calls for other, non- health monitoring purposes.” Id. Dr. Bims testified in his declaration the “cellular monitor 12” described in the ’136 Application had the cellular and wireless circuitry that enabled it to be used as a cellular telephone. Bims 1 Decl. 36—51. Dr. Bims’ testimony is supported by sound scientific reasoning and factual evidence. Id. Accordingly, we find Dr. Bims’ testimony to credibly establish that the 5 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 monitoring apparatus of the ’136 Application could be used to make and receive cellular phone calls for other non-health monitoring purposes. The inquiry as to whether the ’136 Application describes “a multi purpose personal data accessory,” however, does not end with Dr. Bims’ conclusion that monitoring apparatus of the ’136 Application could be utilized as a general purpose cellular phone. In order to be accorded priority under 35 U.S.C. § 120 to a previously filed application, the “invention” must be “disclosed [in the ‘application previously filed in the United States’] in the manner provided by the first paragraph of section 112.” 35 U.S.C. § 120 (pre- AIA). Entitlement to the benefit of the previously filed ’136 Application thus requires that the later-filed claims of the ’878 patent be described in the’ 136 Application in such a way that the written description requirements of 35 U.S.C. § 112 are met. See Tronzo v. Biomet, Inc., 156 F.3d 1154, 1158 (Fed. Cir. 1998) (discussing requirements of claiming benefit of priority date of earlier application under 35 U.S.C. § 120). To satisfy the written description requirement of 35 U.S.C. § 112, the inventor must “convey with reasonable clarity to those skilled in the art that, as of the filing date sought, he or she was in possession of the invention.” Vas-Cath Inc. v. Mahurkar, 935 F.2d 1555, 1563—64 (Fed. Cir. 1991). “One shows that one is ‘in possession’ of the invention by describing the invention, with all its claimed limitations.” Lockwood v. Am. Airlines, Inc., 107 F.3d 1565, 1572 (Fed. Cir. 1997). In describing the claimed invention, there is no requirement that the wording be identical to that used in the specification as long as there is sufficient disclosure to show one of skill in the art that the inventor “invented what is claimed.” Union Oil Co. v. Atlantic Richfield Co., 6 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 208 F.3d 989, 997 (Fed. Cir. 2000). The written description “need not recite the claimed invention in haec verba but [it] must do more than merely disclose that which would render the claimed invention obvious.” ICUMed., Inc. v. Alaris Med. Sys., Inc., 558 F.3d 1368, 1377 (Fed. Cir. 2009). Thus, as long as a person “of ordinary skill in the art would have understood the inventor to have been in possession of the claimed invention at the time of filing, even if every nuance of the claims is not explicitly described in the specification, then the adequate written description requirement is met.” In re Alton, 76 F.3d 1168, 1175 (Fed. Cir. 1996). Thus, the critical inquiry is not whether the monitoring apparatus of the ’136 Application could be utilized as a general purpose cellular phone. Rather, the question is whether the inventors had “possession” of the concept that the monitoring device could be used by the patient as a general purpose cellular telephone. In this case, the only cellular voice function disclosed for the “ambulatory patient monitoring apparatus” described in ’136 Application is to provide “voice communications between the patient and a clinician at the central station.” ’136 Application, col. 1,11. 54—67; col. 2,11. 10-12 (“voice communications circuitry whereby the patient conducts voice communications with a clinician at the central health monitoring station”); col. 4,11. 33—34 (“providing a response step includes voice-communicating an instruction to the patient”). The patient then establishes a communications link between monitor 12 and a central medical monitoring station by dialing via keypad 607 and placing a cellular telephone call which is then connected to the public telephone network. When a clinician at 7 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 the receiving station answers the call the clinician and patient may communication by voice . . . The clinician at the receiving station may analyze the patient's physiological data and may instruct the patient regarding any actions the patient should take . . . Id., col. 8,11. 49-60. Dr. Bims did not provide evidence in his declaration that the ’136 Application describes voice communications between any parties other than the patient and the clinician at the heath monitoring station. Instead, the essence of Dr. Bims testimony is that the cellular circuitry enables and allows the monitoring apparatus to make and receive phone calls from any cell phone or landline. Dr. Bims stated: 52. A person of ordinary skill in the art would have understood that the cellular monitor 12, which communicates with the monitoring station over the public telephone network, could have likewise communicated over the public telephone network with other cellular or landline telephones. The teachings of the Geva Patent certainly do not restrict the purpose of dialing from the keyboard to exclusively placing a call to a clinician, or otherwise forbid using the cellular monitor 12 for placing or receiving phone calls for purposes other than health monitoring. 53. Indeed, the Geva Patent describes that the cellular monitor 12 has a dedicated voice communication channel that is separate from the data channel. From this, the POS A would have understood that the dedicated voice communication channel could be used for communications generally, and was not necessarily restricted to communications exclusively devoted to health care monitoring . . 54. For at least the foregoing reasons, it is my opinion that the POS A in March 1999 would have understood that the Geva Patent described a cellular health monitor that could be used for health monitoring, as well as a general purpose cellular telephone ... In 8 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 other words, the POSA in March 1999 would have understood that the cellular monitor described in the Geva Patent could be used for purposes other than health monitoring. Bims 1 Decl. Tflf 52—54 (emphasis added). Simply because the ’136 Application’s health monitor “could be used for communications generally” and does not “restrict" or “forbid” the patient from using the “ambulatory patient monitoring apparatus” for communication channels other than between patient and doctor (see above) does not mean that the inventors had “possession” of the claimed invention. Vas-Cath, 935 F.2d at 1563—64. “Possession” requires a description of all the claimed features of the invention. Lockwood, 107 F.3d at 1572. Dr. Bims did not provide evidence, or even testily, that the ’136 Application describes the claimed “multi-purpose personal data accessory” having “a function other than health monitoring.” Rather, Dr. Bims merely stated that the ’136 Application does not “restrict" or “forbid” the monitoring apparatus from being used to place and receive calls from other cellular and landlines calls. Bims 1 Decl. 52— 54. Indeed, Dr. Bims repeated states that the cellular health monitor “could be” used a cellular phone, but does not state that it was used for this purpose nor that the inventors recognized it as such. The ’136 Application’s silence as to whether the health monitor could be used as a general purpose cellular telephone {id., 1 54) does not demonstrate “possession” of the claimed “multi purpose personal data accessory” because silence is not a description of “the invention, with all its claimed limitations” as required to comply with the written description requirement 35 U.S.C. § 112, first paragraph. Lockwood, 107 F.3d at 1572. 9 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 While it is true that the ’136 Application does not have to describe the claimed invention in the identical wording utilized in the later filed claims, it must do more than provide disclosure that would have made the claimed invention obvious to one of ordinary skill in the art. Union Oil Co., 208 F.3d at 997; ICU Med., 558 F.3d at 1377. [I]t is the specification itself that must demonstrate possession. And while the description requirement does not demand any particular form of disclosure, Carnegie Mellon Univ. v. Hoffmann- La Roche Inc., 541 F.3d 1115, 1122 (Fed. Cir. 2008), or that the specification recite the claimed invention in haec verba, a description that merely renders the invention obvious does not satisfy the requirement, Lockwood v. Am. Airlines, 107 F.3d 1565, 1571-72 (Fed. Cir. 1997). Ariad Pharmaceuticals, Inc. v. Eli Lilly and Company, 598 F.3d 1336, 1352 (Fed. Cir. 2010). The thrust of Dr. Buns’ testimony is that the health monitor disclosed in the ’136 Application had the necessary cellular components and circuitry so the monitor “could also be used for making and/or receiving call for other, non-health monitoring purposes.” Bims 1 Decl. 136 (emphasis added); see also id., 153 (testifying that the health monitor “could be used for communications generally”). However, while capability to perform a non health care function might have made it obvious to have implemented the function on the disclosed health care monitor, the fact that the monitor in Dr. Bims’ own words “could ... be used ... for other, non-health monitoring purposes” does not establish that the inventors had possession of the non health care function as of the filing date of the ’136 Application. Indeed, we have not been directed to evidence, nor could we find such evidence, that the 10 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 inventors described using the “ambulatory patient monitoring apparatus” of the ’136 Application for a function other than health care monitoring. Patent Owner did not demonstrate the inventors knew, and recognized as part of their invention, that the monitoring apparatus could be used by the patient as a general purpose phone for making phone calls to any desired party. Merely because a later-claimed feature can be deduced from a prior filed application does not establish that the prior filed application describes the feature in such a way that meets the written description requirement of 35 U.S.C. § 112. In Goeddel v. Sugano, 617 F.3d 1350 (2010), the sole count of rgw interference was a “DNA [deoxyribonucleic acid] encoding a mature human fibroblast interferon [“hFIF”] having a total of 166 amino acids of the sequence” which was “unaccompanied by a human fibroblast interferon presequence.” Goeddel, 617 F.3d at 1352. Sugano was awarded priority as to the count of the interference based on the benefit of the filing date of its initial Japanese patent application. Id., 1351. Although the Japanese patent application did not disclose expressly a mature sequence lacking a presequence, the Board of Patent Appeals and Interferences “held that one skilled in this field ‘should have been able to envision’ the DNA molecule that would encode mature hFIF unaccompanied by its presequence”. . . “in view of the Japanese Application’s description of the precursor hFIF and a scientific article by Knight that is referenced in the Japanese Application.” Id., 1354— 55. The Board held the Japanese Application described the mature hFIF of the count because “Knight’s partial sequence of the first 13 amino acids of mature hFIF would allow a person skilled in the field of the invention to 11 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 determine where in the 187 amino acid precursor the presequence ends and the mature sequence begins.” Id. The Court of Appeals to the Federal Circuit, however, held that the Board in Goeddel “erred in ruling that priority is established if a person of skill in the art could ‘envision’ the invention of the counts.” Rather, the court held: That a modified gene encoding the 166 amino acid protein could have been “envisioned” does not establish constructive reduction to practice of the modified gene. The question is not whether one skilled in this field of science might have been able to produce mature hFIF by building upon the teachings of the Japanese Application, but rather whether that application “convey[ed] to those skilled in the art that the inventor had possession of the claimed subject matter as of the filing date.” Ariad Pharm., Inc. v. Eli Lilly & Co., 598 F.3d 1336, 1351 (Fed. Cir. 2010) (en banc); see also Lockwood v. American Airlines, Inc., 107 F.3d 1565, 1572 (Fed. Cir. 1997) (in claiming priority under § 120, “[a] description which renders obvious the invention for which an earlier filing date is sought is not sufficient”); Bradford Co. v. Conteyor North Am., Inc., 603 F.3d 1262, 1269 (Fed. Cir. 2010) (same). Id., 1356 (emphasis added). In this case, Dr. Bims testified that the “ambulatory patient monitoring apparatus” could be used as a general purpose cellular telephone, but Dr. Bims did not explain how such ability conveyed to the ordinary skilled worker that the inventors possessed the concept of utilizing the monitoring apparatus to place and receive phone calls for non-health care purposes. As already discussed “voice communication circuitry” is described in the ’136 Application, but the circuitry is used to communicate with a central health monitoring station. ’136 Application, col. 2,11. 10—12. 12 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 The ’878 patent’s mention of the ’136 Application in the discussion of the ’878 invention is consistent with the conclusion that the Application does not describe “a general purpose cellular telephone.” See Bims 1 Decl. 1 54. The ’878 patent discloses: Various remote medical centers are also known as central medical monitoring stations and are known in the art. Such a center is described at U.S. Pat. No. 6,366,871 [the ’136 Application] titled “Personal ambulatory cellular health monitor for mobile patient” of Geva, which incorporated herein by reference. It is noted that Geva describes a monitor that is capable of vocal communication with the person, and this feature can be implemented by using the cellular phone 210 [of the ’878 patent; see ’878 patent, col. 6,11. 5—7]. ’878 patent, col. 8,11. 10-17. The ’878 patent does not characterize the cellular health monitor of the ’136 Application as a cellular phone, but rather states that the voice communication in the Application can be “implemented” with the cellular phone 210 of the ’878 patent (see e.g., Fig. 3 showing cellular phone 210). This cited disclosure serves as additional independent evidence that the inventors later recognized, only after filing the application that led to the ’878 patent, that a general purpose cellular telephone used to place and receive phone calls for non-health care purposes could be used in place of the voice communications circuitry of the ’136 Application (see ’136 Application, col. 2,11. 1-21). SUMMARY The Examiner’s decision to deny claims 1, 31, 34, 46, and 37 the benefit of the filing date of the ’136 Application is affirmed. 13 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 All the prior rejections fall with the decision to deny the ’878 patent the March 3, 1999 filing date of the ’136 Application (see Answer 9). TIME PERIOD FOR RESPONSE Requests for extensions of time in this ex parte reexamination proceeding are governed by 37 C.F.R. § 1.550(c). See 37 C.F.R. § 41.50(f). AFFIRMED 14 Appeal 2012-010812 Application 12/706,541 Reexamination Control 90/010,751 Patent U.S. 7,542,878 B2 Patent Owner: BRINKS HOFER GILSON & LIONE P.O. BOX 10395 CHICAGO, IL 60610 Third Party Requester: HARRITY & HARRITY, LLP 11350 RANDOM HILLS ROAD, SUITE 600 FAIRFAX, VA 22030 15 Copy with citationCopy as parenthetical citation