CHOLANGIOLAPCATH(TM)

CHOLANGIOLAPCATH(TM) is an FDA 510(k)-cleared medical device (K921091) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 5, 1992. Regulation: 8.