RUSCH MANUAL RESUSCITATOR BAG

RUSCH MANUAL RESUSCITATOR BAG is an FDA 510(k)-cleared medical device (K993194) manufactured by Rusch, 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 23, 2000. Regulation: 8.