Medilaser-S Mel-444-S

K840739 is the FDA 510(k) clearance record for MEDILASER-S MEL-444-S, a class II device, cleared for Mochida Pharmaceutical Co., Ltd. on 1984-09-20 under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list 4 510(k) clearances for Mochida Pharmaceutical Co., Ltd., from 1984-09-20 to 2024-06-21. As of 2026-09-10, FDA records show no recalls naming K840739.