AirLife Autofill Humidification Chamber

AirLife Autofill Humidification Chamber is an FDA 510(k)-cleared medical device (K160764) manufactured by Carefusion 2200, 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 August 24, 2016. Regulation: 8.