Adi 9000/9001 Arthroscope and Accessories

K992621 is the FDA 510(k) clearance record for ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES, a class II device, cleared for Advanced Diagnostics & Interventions on 1999-11-08 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 one 510(k) clearance for Advanced Diagnostics & Interventions. As of 2026-09-10, FDA records show no recalls naming K992621.