MODIFICATION OF AUTOTRANSFUSION APPARATUS (AUTOLOG)

MODIFICATION OF AUTOTRANSFUSION APPARATUS (AUTOLOG) is an FDA 510(k)-cleared medical device (K982755) manufactured by Medtronic Blood Management. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 19, 1998. Regulation: 8.