PURITAN-BENNET INFANT MANUAL RESUSCITATOR MODIFIED

PURITAN-BENNET INFANT MANUAL RESUSCITATOR MODIFIED is an FDA 510(k)-cleared medical device (K920570) manufactured by Puritan Bennett 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 February 26, 1992. Regulation: 8.