Isi Metzenbaum Scissors

K934075 is the FDA 510(k) clearance record for ISI METZENBAUM SCISSORS, a class II device, cleared for Innovative Surgical, Inc. on 1993-12-01 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 Innovative Surgical, Inc., from 1993-08-19 to 1995-01-27. As of 2026-09-10, FDA records show no recalls naming K934075.