Sharplan Model 1120 CO2 Surgical Laser

K936109 is the FDA 510(k) clearance record for SHARPLAN MODEL 1120 CO2 SURGICAL LASER, a class II device, cleared for Sharplan Lasers, Inc. on 1994-05-17 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 78 510(k) clearances for Sharplan Lasers, Inc., from 1986-04-24 to 1997-12-04. As of 2026-09-10, FDA records show no recalls naming K936109.