CANDELA LONG PULSE ND:YAG

CANDELA LONG PULSE ND:YAG is an FDA 510(k)-cleared medical device (K010104) manufactured by Candela Corp.. 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 10, 2001. Regulation: 8.