HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR

HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR is an FDA 510(k)-cleared medical device (K964719) manufactured by Hudson Respiratory Care, 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 February 20, 1997. Regulation: 8.