Section 884.4100 - Endoscopic electrocautery and accessories(a)Identification. An endoscopic electrocautery is a device used to perform female sterilization under endoscopic observation. It is designed to coagulate fallopian tube tissue with a probe heated by low-voltage energy. This generic type of device may include the following accessories: electrical generators, probes, and electrical cables.(b)Classification. Class II. The special controls for this device are:(1) FDA's:(i) "Use of International Standard ISO 10993 'Biological Evaluation of Medical Devices-Part I: Evaluation and Testing,' "(ii) "510(k) Sterility Review Guidance 2/12/90 (K-90)," and(iii) "Guidance ('Guidelines') for Evaluation of Laproscopic Bipolar and Thermal Coagulators (and Accessories),"(2) International Electrotechnical Commission's IEC 60601-1-AM2 (1995-03), Amendment 2, "Medical Electrical Equipment-Part 1: General Requirements for Safety,"(3) American National Standards Institute/American Association for Medical Instrumentation's HF-18, 1993, "Electrosurgical Devices,"(4) Labeling:(i) Indication: For female tubal sterilization, and(ii) Instructions for use:(A) Destroy at least 2 centimeters of the fallopian tubes,(B) Use a cut or undampened sinusoidal waveform,(C) Use a minimum power of 25 watts, and(D) For devices with ammeters: continue electrode activation for 5 seconds after the visual endpoint (tissue blanching) is reached or current flow ceases indicating adequate tissue destruction.45 FR 12684, Feb. 26, 1980, as amended at 52 FR 17741, May 11, 1987; 65 FR 17146, Mar. 31, 2000