
Edwards Lifesciences Research Medical
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18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II is an FDA 510(k)-cleared medical device (K073559) manufactured by Edwards Lifesciences Research Medical. 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 30, 2008. Regulation: 8.