ABI VEST AIRWAY CLEARANCE SYSTEM

ABI VEST AIRWAY CLEARANCE SYSTEM is an FDA 510(k)-cleared medical device (K993629) manufactured by American Biosystems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 20, 2000. Regulation: 8.