Inlet Irrigation/aspiration Valve and Probes

K923528 is the FDA 510(k) clearance record for INLET IRRIGATION/ASPIRATION VALVE AND PROBES, a class II device, cleared for Inlet Medical, Inc. on 1993-01-12 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 2 510(k) clearances for Inlet Medical, Inc., from 1993-01-12 to 1999-06-03. As of 2026-09-10, FDA records show no recalls naming K923528.