Atl CO2 Medical Laser Systems, Models Atl-150 and Atl-250

K083918 is the FDA 510(k) clearance record for ATL CO2 MEDICAL LASER SYSTEMS, MODELS ATL-150 AND ATL-250, a class II device, cleared for Advanced Technology Laser Co., Ltd. on 2009-02-02 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 5 510(k) clearances for Advanced Technology Laser Co., Ltd., from 2009-01-29 to 2014-10-08. As of 2026-09-10, FDA records show no recalls naming K083918.