CABLECAP MODEL: WLF, STZ, ACM

CABLECAP MODEL: WLF, STZ, ACM is an FDA 510(k)-cleared medical device (K101496) manufactured by Sensormed. 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 September 13, 2010. Regulation: 8.