PURITAN-BENNETT DISPOSABLE MANUAL RESUSCITATOR (DMR)

PURITAN-BENNETT DISPOSABLE MANUAL RESUSCITATOR (DMR) is an FDA 510(k)-cleared medical device (K944347) 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 December 11, 1994. Regulation: 8.