Nobles-Lai Endoscopic/laparoscopic

K933345 is the FDA 510(k) clearance record for NOBLES-LAI ENDOSCOPIC/LAPAROSCOPIC, a class II device, cleared for Nobles-Lai Engineering, Inc. on 1994-02-22 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 5 510(k) clearances for Nobles-Lai Engineering, Inc., from 1990-02-26 to 1995-10-18. As of 2026-09-10, FDA records show no recalls naming K933345.