UMBILICAL ARTERY OXYGEN SENSOR

UMBILICAL ARTERY OXYGEN SENSOR is an FDA 510(k)-cleared medical device (K875225) manufactured by Ohmeda Medical. 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 3, 1988. Regulation: 8.