HEMOVAC AUTOTRANSFUSION SYSTEM

HEMOVAC AUTOTRANSFUSION SYSTEM is an FDA 510(k)-cleared medical device (K920273) manufactured by Zimmer Patient Care Division. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 1993. Regulation: 8.