Yesng Reusable Electrosurgical Handle

K881408 is the FDA 510(k) clearance record for YESNG REUSABLE ELECTROSURGICAL HANDLE, a class II device, cleared for Ferguson Medical on 1988-04-14 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 57 510(k) clearances for Ferguson Medical, from 1985-10-29 to 2004-04-23. As of 2026-09-10, FDA records show no recalls naming K881408.