Instruments for Endoscopic Subfascial Harvesting of Veins (Eshv), Instruments for Endoscopic Subfascial Discision of per

K973943 is the FDA 510(k) clearance record for INSTRUMENTS FOR ENDOSCOPIC SUBFASCIAL HARVESTING OF VEINS (ESHV), INSTRUMENTS FOR ENDOSCOPIC SUBFASCIAL DISCISION OF PER, a class II device, cleared for Richard Wolf Medical Instruments Corp. on 1998-08-27 under FDA product code GCJ (Laparoscope, General & Plastic Surgery). FDA's definition for product code GCJ reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 153 510(k) clearances for Richard Wolf Medical Instruments Corp., from 1977-03-07 to 2024-06-03. As of 2026-09-10, FDA records show no recalls naming K973943.