HEPARINIZED ARTERIAL SCREEN BLOOD FILTER

HEPARINIZED ARTERIAL SCREEN BLOOD FILTER is an FDA 510(k)-cleared medical device (K900758) manufactured by Cobe Laboratories, 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 May 16, 1990. Regulation: 8.