Pulsemaster 1000 St Dental Laser System

K972325 is the FDA 510(k) clearance record for PULSEMASTER 1000 ST DENTAL LASER SYSTEM, a class II device, cleared for American Dental Technologies, Inc. on 1997-09-19 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 8 510(k) clearances for American Dental Technologies, Inc., from 1995-08-10 to 2003-04-15. As of 2026-09-10, FDA records show no recalls naming K972325.