Duowipe Cautery Tip & Instrument Cleaner

K830277 is the FDA 510(k) clearance record for DUOWIPE CAUTERY TIP & INSTRUMENT CLEANER, a class II device, cleared for Ritmed, Inc. on 1983-03-08 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI 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 Ritmed, Inc., from 1983-02-28 to 1984-02-17. As of 2026-09-10, FDA records show no recalls naming K830277.