Bipolar Coagulating Forceps

K811820 is the FDA 510(k) clearance record for BIPOLAR COAGULATING FORCEPS, a class II device, cleared for New England Surgical Instrument Corp. on 1981-07-28 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 18 510(k) clearances for New England Surgical Instrument Corp., from 1981-07-28 to 1989-09-15. As of 2026-09-10, FDA records show no recalls naming K811820.