Laparoscopic Instrument, Electrode and Cable

K032965 is the FDA 510(k) clearance record for LAPAROSCOPIC INSTRUMENT, ELECTRODE AND CABLE, a class II device, cleared for Modern Medical Equipment Mfg., Ltd. on 2004-05-13 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI 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 14 510(k) clearances for Modern Medical Equipment Mfg., Ltd., from 2003-02-27 to 2010-05-19. As of 2026-09-10, FDA records show no recalls naming K032965.