PALOMAR LUX2940 HANDPIECE

PALOMAR LUX2940 HANDPIECE is an FDA 510(k)-cleared medical device (K063571) manufactured by Palomar Medical Technologies, 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 February 8, 2007. Regulation: 8.