VENTILATOR, EMERGENCY, MANUAL (RESUSCITATOR)

VENTILATOR, EMERGENCY, MANUAL (RESUSCITATOR) is an FDA 510(k)-cleared medical device (K954150) manufactured by Green Field Medical Sourcing, 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 December 19, 1995. Regulation: 8.