AMBU SINGLE PATIENT USE PEEP VALVE

AMBU SINGLE PATIENT USE PEEP VALVE is an FDA 510(k)-cleared medical device (K923976) 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 January 4, 1993. Regulation: 8.