Slt Prism/refracting Probe

K934208 is the FDA 510(k) clearance record for SLT PRISM/REFRACTING PROBE, a class II device, cleared for Surgical Laser Technologies, Inc. on 1994-08-26 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 51 510(k) clearances for Surgical Laser Technologies, Inc., from 1985-05-10 to 2004-11-08. As of 2026-09-10, FDA records show no recalls naming K934208.