Ktp/532 & Ktp/yag Surgical Lasers

K913244 is the FDA 510(k) clearance record for KTP/532 & KTP/YAG SURGICAL LASERS, a class II device, cleared for Charles L. Rose and Co., Inc. on 1992-07-28 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 4 510(k) clearances for Charles L. Rose and Co., Inc., from 1990-09-05 to 1992-07-28. As of 2026-09-10, FDA records show no recalls naming K913244.