AMBU MEDIBAG ADULT, AMBU MEDIBAG INFANT/CHILD

AMBU MEDIBAG ADULT, AMBU MEDIBAG INFANT/CHILD is an FDA 510(k)-cleared medical device (K982722) manufactured by Ambu, 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 April 11, 1999. Regulation: 8.