SMARTLITE D FREQUENCY DOUBLED ND:YAG LASER

SMARTLITE D FREQUENCY DOUBLED ND:YAG LASER is an FDA 510(k)-cleared medical device (K040289) manufactured by Cynosure, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 2004. Regulation: 8.