Acutome(r) 150 Multi-Wavelength Color-Corrected(tm) Laser Handpiece

K950215 is the FDA 510(k) clearance record for ACUTOME(R) 150 MULTI-WAVELENGTH COLOR-CORRECTED(TM) LASER HANDPIECE, a class II device, cleared for Reliant Laser Corp. on 1995-06-15 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 3 510(k) clearances for Reliant Laser Corp., from 1992-05-21 to 1995-06-15. As of 2026-09-10, FDA records show no recalls naming K950215.