DLP Silicone Coronary Artery Ostial Cannulae

DLP Silicone Coronary Artery Ostial Cannulae is an FDA 510(k)-cleared medical device (K231206) 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 December 6, 2023. Regulation: 8.