Model Mc 1100 Surgical Yag Laser

K903943 is the FDA 510(k) clearance record for MODEL MC 1100 SURGICAL YAG LASER, a class II device, cleared for Klinger Micro-Controle Group on 1990-11-21 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 one 510(k) clearance for Klinger Micro-Controle Group. As of 2026-09-10, FDA records show no recalls naming K903943.