CLEARFLASH AC2100 COSMETIC SYSTEM

CLEARFLASH AC2100 COSMETIC SYSTEM is an FDA 510(k)-cleared medical device (K111937) manufactured by Clearflash 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 7, 2012. Regulation: 8.