MODIFICATION TO RESQPOD CIRCULATORY ENHANCER

MODIFICATION TO RESQPOD CIRCULATORY ENHANCER is an FDA 510(k)-cleared medical device (K033401) manufactured by Advanced Circulatory Systems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 19, 2003. Regulation: 8.