Centauri Yag Laser Syst, Ophthamology

K904630 is the FDA 510(k) clearance record for CENTAURI YAG LASER SYST, OPHTHAMOLOGY, a class II device, cleared for Pfizer Laser Systems on 1990-12-17 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 32 510(k) clearances for Pfizer Laser Systems, from 1988-05-11 to 1993-11-16. As of 2026-09-10, FDA records show no recalls naming K904630.