Ex Parte DaltonDownload PDFBoard of Patent Appeals and InterferencesMay 4, 201011049488 (B.P.A.I. May. 4, 2010) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE ____________________ BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES ____________________ Ex parte MICHAEL J. DALTON ____________________ Appeal 2009-007870 Application 11/049,488 Technology Center 3700 ____________________ Decided: May 5, 2010 ____________________ Before: WILLIAM F. PATE III, LINDA E. HORNER, and MICHAEL W. O'NEILL, Administrative Patent Judges. PATE III, Administrative Patent Judge. DECISION ON APPEAL STATEMENT OF CASE Appellant appeals under 35 U.S.C. § 134 from a rejection of claims 1- 20. App. Br 5. We have jurisdiction under 35 U.S.C. § 6(b). The claims are directed to needle safety and protection device. Claim 1, reproduced below, is illustrative of the claimed subject matter: Appeal 2009-007870 Application 11/049,488 2 1. A fluid delivery device comprising: a fluid delivery tube; a needle received within a distal portion of the fluid delivery tube; a planar base mounted to the fluid delivery tube adjacent a distal portion of the fluid delivery tube; and a planar shield connected at one end to the base with a flexible connection, the shield having an adhesive portion located on an outer surface, wherein in an insertion configuration the planar base and the planar shield are substantially parallel to the fluid delivery tube and the needle fits through a shield aperture and the adhesive portion is adapted to contact a target skin region, and wherein in a protection configuration a needle tip contacts a portion of an inner surface of the planar shield spaced apart from the shield aperture and wherein the planar base remains substantially parallel to the fluid delivery tube. REFERENCES The prior art relied upon by the Examiner in rejecting the claims on appeal is: Wanderer Szerlip Gyure Rosato US 4,850,961 US 5,364,370 US 5,681,295 US 5,951,522 Jul. 25, 1989 Nov. 15, 1994 Oct. 28, 1997 Sep. 14, 1999 REJECTIONS Claims 1-5 and 17-19 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Szerlip and Wanderer. Ans. 3. Appeal 2009-007870 Application 11/049,488 3 Claims 6-9 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Szerlip, Wanderer, and Gyure. Ans. 4. Claims 10-16 and 20 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Szerlip, Wanderer, and Rosato. Ans. 5. OPINION Appellant contends that the Examiner erred by finding that Szerlip and Wanderer would have taught or suggested the “planar shield” recited in claims 1, 10 and 17. Reply Br. 5. Appellant also contends that the Examiner erred by finding that Szerlip and Wanderer would have taught or suggested the planar base and planar shield “substantially parallel to the fluid delivery tube” in an insertion configuration as recited in claims 1 and 10. App. Br. 11. Both of Appellant’s contentions are correct. The Supreme Court in KSR reaffirmed the framework for determining obviousness as set forth in Graham v. John Deere Co. (383 U.S. 1 (1966)). The factual inquiries set forth in Graham that are applied for establishing a background for determining obviousness under 35 U.S.C. § 103(a) are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. Szerlip’s helical springs 22, 32 are not planar and are therefore not reasonably read as the claimed “planar shield.” Szerlip col. 4, ll. 15-18, col. Appeal 2009-007870 Application 11/049,488 4 5, ll. 1-4; Contra Ans. 3. It would have been reasonable to read planar surfaces or faces 24, 40 of Szerlip’s cap 16, 30 as the claimed “planar shield.” These surfaces are perpendicular to the tube of syringe 34, read as the “fluid delivery tube.” “Perpendicular” to a tube would be understood by one of ordinary skill in the art to mean perpendicular to the longitudinal axis of that tube. It is further noted that the distal portion of the syringe 34 is read as the claimed “planar base.” Ans. 3. While this interpretation may be reasonable, this structure can not then also serve as part of the structure read as the claimed “fluid delivery tube.” The structure read as the claimed “fluid delivery tube” therefore includes essentially only a longitudinal portion. Since Szerlip’s perpendicular cap face is not “substantially parallel” to the tube, and Wanderer does not cure this deficiency, the combination of Szerlip and Wanderer would not have taught or suggested the planar base and planar shield “substantially parallel to the fluid delivery tube” in an insertion configuration as recited in claims 1 and 10. Szerlip’s planar surfaces or faces 24, 40 would also fail to meet the “planar shield directly connected at one end to the base” of claim 17, since they are connected to the base, the distal end of the syringe, by intermediate members, springs 22, 32. Neither Gyure nor Rosato, as applied by the Examiner, cure the deficiencies of Szerlip and Wanderer. Since the Examiner relied upon an unreasonable interpretation of the claim terms in determining the differences between the prior art and the claims at issue, we are constrained to reverse the rejections of claims 1, 10 and 17 along with dependent claims 2-9, 11-16 and 18-20. Appeal 2009-007870 Application 11/049,488 5 DECISION For the above reasons, the Examiner’s rejection of claims 1-20 are reversed. REVERSED vsh/nhl CARDINAL LAW GROUP SUITE 2000 1603 ORRINGTON AVENUE EVANSTON IL 60201 Copy with citationCopy as parenthetical citation