RESERVOIR FOR AUTOLOGOUS BLOOD TRANSFUS.

RESERVOIR FOR AUTOLOGOUS BLOOD TRANSFUS. is an FDA 510(k)-cleared medical device (K802674) manufactured by Haemonetics Corp.. 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 7, 1981. Regulation: 8.