NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY

NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY is an FDA 510(k)-cleared medical device (K895149) manufactured by Shiley, 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 November 27, 1989. Regulation: 8.