RESUBMITTED MULTIORGAN PERFUSION CANNULA

RESUBMITTED MULTIORGAN PERFUSION CANNULA is an FDA 510(k)-cleared medical device (K902394) manufactured by Fresenius USA, 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 26, 1990. Regulation: 8.