PALOMAR LUX1540 HANDPIECE

PALOMAR LUX1540 HANDPIECE is an FDA 510(k)-cleared medical device (K060301) 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 March 22, 2006. Regulation: 8.