PASTELLE Q-SWITCHED ND: YAG LASER

PASTELLE Q-SWITCHED ND: YAG LASER is an FDA 510(k)-cleared medical device (K123293) manufactured by Won Technology Co., Ltd.. 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, 2013. Regulation: 8.