AED Arthroscope

K991656 is the FDA 510(k) clearance record for AED ARTHROSCOPE, a class II device, cleared for National Advanced Endoscopy Devices, Inc. on 1999-12-02 under FDA product code HRX (Arthroscope). FDA's definition for product code HRX 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 8 510(k) clearances for National Advanced Endoscopy Devices, Inc., from 1999-12-02 to 2017-08-01. As of 2026-09-10, FDA records show no recalls naming K991656.