RMI ARTERIAL PERFUSION CANNULA

RMI ARTERIAL PERFUSION CANNULA is an FDA 510(k)-cleared medical device (K894243) manufactured by Research 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 September 18, 1989. Regulation: 8.