Cutting and Coagulation Devices and Accessories

K921696 is the FDA 510(k) clearance record for CUTTING AND COAGULATION DEVICES AND ACCESSORIES, a class II device, cleared for American Cyanamid Co. on 1992-11-18 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 7 510(k) clearances for American Cyanamid Co., from 1983-06-15 to 1993-12-17. As of 2026-09-10, FDA records show no recalls naming K921696.