MADTRONIC DLP ARTERIAL CANNULAE

MADTRONIC DLP ARTERIAL CANNULAE is an FDA 510(k)-cleared medical device (K991066) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 1999. Regulation: 8.