VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)

VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL) is an FDA 510(k)-cleared medical device (K063217) manufactured by B.Braun Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2007. Regulation: 8.