Model 5202 Micromanipulator

K874811 is the FDA 510(k) clearance record for MODEL 5202 MICROMANIPULATOR, a class II device, cleared for Coherent Medical Group on 1988-02-05 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 27 510(k) clearances for Coherent Medical Group, from 1985-01-03 to 1997-01-22. As of 2026-09-10, FDA records show no recalls naming K874811.