BAYLOR RAPID AUTOTRANSFUSION SYSTEM

BAYLOR RAPID AUTOTRANSFUSION SYSTEM is an FDA 510(k)-cleared medical device (K852736) manufactured by Cardio Systems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 1985. Regulation: 8.