AIRLIFE BUBBLE HUMIDIFER, MODEL 002003 AND 002006

AIRLIFE BUBBLE HUMIDIFER, MODEL 002003 AND 002006 is an FDA 510(k)-cleared medical device (K991484) manufactured by Allegiance Healthcare Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 12, 1999. Regulation: 8.