Aurora M Medical Dye Laser

K855246 is the FDA 510(k) clearance record for AURORA M MEDICAL DYE LASER, a class II device, cleared for Cooper Lasersonics, Inc. on 1986-03-21 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 54 510(k) clearances for Cooper Lasersonics, Inc., from 1982-09-13 to 1988-04-18. As of 2026-09-10, FDA records show no recalls naming K855246.