BAUMAN CPR/RESUSCITATOR

BAUMAN CPR/RESUSCITATOR is an FDA 510(k)-cleared medical device (K904346) manufactured by General Medical Products, 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 October 1, 1990. Regulation: 8.