Scanlan(r) Thoracoscopic Scissors, Clamp, Forceps, Needle Holder

K945474 is the FDA 510(k) clearance record for SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER, a class II device, cleared for Scanlan Intl., Inc. on 1994-12-05 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 19 510(k) clearances for Scanlan Intl., Inc., from 1978-04-18 to 1996-04-26. As of 2026-09-10, FDA records show no recalls naming K945474.