Smith & Nephew Dyonics Arthoscopes/endoscopes, Smith & Nephew Dyonics Laparoscopes, Snith & Nephew Dyonics Hysteroscopes

K974767 is the FDA 510(k) clearance record for SMITH & NEPHEW DYONICS ARTHOSCOPES/ENDOSCOPES, SMITH & NEPHEW DYONICS LAPAROSCOPES, SNITH & NEPHEW DYONICS HYSTEROSCOPES, a class II device, cleared for Endoscopy Division on 1998-01-23 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 one 510(k) clearance for Endoscopy Division. As of 2026-09-10, FDA records show no recalls naming K974767.