BD Centro Vena Acute Central Line (7 French Dual Lumen)

BD Centro Vena Acute Central Line (7 French Dual Lumen) is an FDA 510(k)-cleared medical device (K200266) manufactured by Bard Access Systems, Inc. (Bard Has Joined Bd). This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 6, 2020. Regulation: 8.