ARGYLE SENTINEL SEAL AUTOTRANSFUSION SYSTEM

ARGYLE SENTINEL SEAL AUTOTRANSFUSION SYSTEM is an FDA 510(k)-cleared medical device (K864374) 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 March 15, 1987. Regulation: 8.