PALOMAR ASPIRE LASER PLATFORM

PALOMAR ASPIRE LASER PLATFORM is an FDA 510(k)-cleared medical device (K081416) manufactured by Palomar Medical Products, 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 May 28, 2008. Regulation: 8.