Arthroscope-Various Models Fiberoptic

K832341 is the FDA 510(k) clearance record for ARTHROSCOPE-VARIOUS MODELS FIBEROPTIC, a class II device, cleared for Kamiya Tsusan Kaisha, Ltd. on 1983-10-04 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 4 510(k) clearances for Kamiya Tsusan Kaisha, Ltd., from 1983-08-12 to 1986-09-05. As of 2026-09-10, FDA records show no recalls naming K832341.