Retraction Instrument

K921103 is the FDA 510(k) clearance record for RETRACTION INSTRUMENT, a class II device, cleared for Origin Medsystems, Inc. on 1993-09-09 under FDA product code GCJ (Laparoscope, General & Plastic Surgery). FDA's definition for product code GCJ 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 50 510(k) clearances for Origin Medsystems, Inc., from 1989-12-27 to 1999-07-30. As of 2026-09-10, FDA records show no recalls naming K921103.