Duostar

K974170 is the FDA 510(k) clearance record for DUOSTAR, a class II device, cleared for Mti Corp./ Electrostar S.A.-Haiti on 1998-09-30 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 one 510(k) clearance for Mti Corp./ Electrostar S.A.-Haiti. As of 2026-09-10, FDA records show no recalls naming K974170.