INTERFACE ARTERIAL BLOOD FILTER, MODEL 42

INTERFACE ARTERIAL BLOOD FILTER, MODEL 42 is an FDA 510(k)-cleared medical device (K862591) manufactured by 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 3, 1986. Regulation: 8.