CUTERA OPTIONAL PULSED LIGHT HAND PIECE FAMILY

CUTERA OPTIONAL PULSED LIGHT HAND PIECE FAMILY is an FDA 510(k)-cleared medical device (K050047) 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 30, 2005. Regulation: 8.