ANTLIA II SUCTION PUMP SYSTEM

ANTLIA II SUCTION PUMP SYSTEM is an FDA 510(k)-cleared medical device (K070904) manufactured by Innovative Therapies, 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 April 12, 2007. Regulation: 8.