Burton H- Base Table - Model 1990

K924773 is the FDA 510(k) clearance record for BURTON H- BASE TABLE - MODEL 1990, a class II device, cleared for R.H. Burton Co. on 1993-06-07 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 19 510(k) clearances for R.H. Burton Co., from 1992-05-07 to 1993-06-07. As of 2026-09-10, FDA records show no recalls naming K924773.