Surgilase CO2 Surgical Laser System Model Sl80

K884092 is the FDA 510(k) clearance record for SURGILASE CO2 SURGICAL LASER SYSTEM MODEL SL80, a class II device, cleared for Surgilase, Inc. on 1988-10-13 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 19 510(k) clearances for Surgilase, Inc., from 1985-11-13 to 1993-10-15. As of 2026-09-10, FDA records show no recalls naming K884092.