REVLITE Q-SWITCHED ND:YAG LASER

REVLITE Q-SWITCHED ND:YAG LASER is an FDA 510(k)-cleared medical device (K063112) manufactured by Hoya Conbio, 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 November 30, 2006. Regulation: 8.