CYNOSURE YAG FAMILY LASER

CYNOSURE YAG FAMILY LASER is an FDA 510(k)-cleared medical device (K072484) 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 December 26, 2007. Regulation: 8.