Ktp/532 Surgical Laser for Percutaneous Diskectomy

K896183 is the FDA 510(k) clearance record for KTP/532 SURGICAL LASER FOR PERCUTANEOUS DISKECTOMY, a class II device, cleared for Laserscope on 1990-02-02 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 60 510(k) clearances for Laserscope, from 1985-06-18 to 2006-12-01. As of 2026-09-10, FDA records show no recalls naming K896183.