MONITOR, CITADEL INTRAVASCULAR PO2

MONITOR, CITADEL INTRAVASCULAR PO2 is an FDA 510(k)-cleared medical device (K760350) manufactured by Sherwood Medical Industries. 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 28, 1976. Regulation: 8.