MANUAL PULMONARY RESUSICITATOR

MANUAL PULMONARY RESUSICITATOR is an FDA 510(k)-cleared medical device (K953546) manufactured by Medical Marketing Concepts. 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 28, 1996. Regulation: 8.