Bovie X-10 Electrosurgical Generator(unit)

K844565 is the FDA 510(k) clearance record for BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT), a class II device, cleared for Clinical Technology Corp. on 1985-02-21 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 12 510(k) clearances for Clinical Technology Corp., from 1982-01-22 to 1994-01-31. As of 2026-09-10, FDA records show no recalls naming K844565.