DLP CORONARY OSTIAL PERFUSION CANNULAE

DLP CORONARY OSTIAL PERFUSION CANNULAE is an FDA 510(k)-cleared medical device (K131269) manufactured by Medtronic, 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 July 9, 2013. Regulation: 8.