ARGYLE AUTOTRANSFUSION BAG

ARGYLE AUTOTRANSFUSION BAG is an FDA 510(k)-cleared medical device (K882757) manufactured by Sherwood Medical Co.. 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 31, 1988. Regulation: 8.