BARD-PARKER ARTERIAL MONITORING SYSTEM

BARD-PARKER ARTERIAL MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K780939) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 16, 1978. Regulation: 8.