Percscope Model 2600

K974579 is the FDA 510(k) clearance record for PERCSCOPE MODEL 2600, a class II device, cleared for Clarus Medical Systems, Inc. on 1998-02-18 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 22 510(k) clearances for Clarus Medical Systems, Inc., from 1992-11-16 to 1998-08-18. As of 2026-09-10, FDA records show no recalls naming K974579.