Meditec Ql-15 Nd:yag Laser

K884060 is the FDA 510(k) clearance record for MEDITEC QL-15 ND:YAG LASER, a class II device, cleared for Storz Ophthalmics, Inc. on 1988-11-04 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 2 510(k) clearances for Storz Ophthalmics, Inc., from 1988-11-04 to 1995-03-02. As of 2026-09-10, FDA records show no recalls naming K884060.