Rd-1200H Normal Mode Ruby Laser System

K955612 is the FDA 510(k) clearance record for RD-1200H NORMAL MODE RUBY LASER SYSTEM, a class II device, cleared for Spectrum Medical Technologies, Inc. on 1996-07-09 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 Spectrum Medical Technologies, Inc., from 1992-04-21 to 1997-03-05. As of 2026-09-10, FDA records show no recalls naming K955612.