HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C.

HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C. is an FDA 510(k)-cleared medical device (K852464) manufactured by Hcg, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 1985. Regulation: 8.