Forceps for Laparoscopic Surgery Gu Use

K925959 is the FDA 510(k) clearance record for FORCEPS FOR LAPAROSCOPIC SURGERY GU USE, a class II device, cleared for Zinnanti Surgical Instruments, Inc. on 1993-11-12 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 76 510(k) clearances for Zinnanti Surgical Instruments, Inc., from 1984-06-15 to 1997-06-13. As of 2026-09-10, FDA records show no recalls naming K925959.