Copper Vapor Laser System

K915370 is the FDA 510(k) clearance record for COPPER VAPOR LASER SYSTEM, a class II device, cleared for Metatech Corp. on 1992-02-07 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 16 510(k) clearances for Metatech Corp., from 1985-04-03 to 2004-04-30. As of 2026-09-10, FDA records show no recalls naming K915370.