Reprocessed Surgical Scissors and Graspers

K033592 is the FDA 510(k) clearance record for REPROCESSED SURGICAL SCISSORS AND GRASPERS, a class II device, cleared for Clearmedical, Inc. on 2004-07-27 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 Clearmedical, Inc., from 2002-02-06 to 2005-07-11. As of 2026-09-10, FDA records show no recalls naming K033592.