MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR

MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR is an FDA 510(k)-cleared medical device (K895196) manufactured by Nidek, 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 October 15, 1989. Regulation: 8.