Applied Optronics Model Aoc 5060 Surgfical Diode Laser System

K955007 is the FDA 510(k) clearance record for APPLIED OPTRONICS MODEL AOC 5060 SURGFICAL DIODE LASER SYSTEM, a class II device, cleared for Applied Optronics Corp. on 1996-01-26 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 4 510(k) clearances for Applied Optronics Corp., from 1996-01-26 to 1996-11-01. As of 2026-09-10, FDA records show no recalls naming K955007.