Unipolar Coagulator Probe System

K911274 is the FDA 510(k) clearance record for UNIPOLAR COAGULATOR PROBE SYSTEM, a class II device, cleared for American Surgical Instruments Corp. on 1991-06-20 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 6 510(k) clearances for American Surgical Instruments Corp., from 1990-03-28 to 1993-11-08. As of 2026-09-10, FDA records show no recalls naming K911274.