CUTERA ER:YAG LASER HANDPIECE

CUTERA ER:YAG LASER HANDPIECE is an FDA 510(k)-cleared medical device (K070138) manufactured by Cutera, 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 March 26, 2007. Regulation: 8.