INTERSEPT* CARDIOTOMY RESERVOIR WITH FILTER

INTERSEPT* CARDIOTOMY RESERVOIR WITH FILTER is an FDA 510(k)-cleared medical device (K864895) manufactured by Johnson & Johnson Professionals, 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 February 18, 1987. Regulation: 8.