DMR PLUS DISPOSABLE MANUAL RESUSCITATOR

DMR PLUS DISPOSABLE MANUAL RESUSCITATOR is an FDA 510(k)-cleared medical device (K973419) manufactured by Nellcor Puritan Bennett, 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 March 24, 1998. Regulation: 8.