INFANT PERCUSSOR #5534

INFANT PERCUSSOR #5534 is an FDA 510(k)-cleared medical device (K812803) manufactured by Hudson Oxygen Therapy Sales Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 2, 1981. Regulation: 8.