Model 305Aa Portable Laser

K841781 is the FDA 510(k) clearance record for MODEL 305AA PORTABLE LASER, a class II device, cleared for Laser Spectrum, Inc. on 1984-11-07 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 5 510(k) clearances for Laser Spectrum, Inc., from 1984-04-23 to 1986-10-06. As of 2026-09-10, FDA records show no recalls naming K841781.