MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING

MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING is an FDA 510(k)-cleared medical device (K905464) manufactured by Angiosystems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 30, 1991. Regulation: 8.