AMBIENT TURBOFLASH 90 IFS

AMBIENT TURBOFLASH 90 IFS is an FDA 510(k)-cleared medical device (K120791) manufactured by Arthocare Corporation. 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 December 10, 2012. Regulation: 8.