Multiple CO2 Laers

K941838 is the FDA 510(k) clearance record for MULTIPLE CO2 LAERS, a class II device, cleared for Mattioli Engineering, Srl on 1994-12-15 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 Mattioli Engineering, Srl, from 1994-12-15 to 2010-03-10. As of 2026-09-10, FDA records show no recalls naming K941838.