CIRCUFLOW 5200 SEQUENTIAL COMPRESSION DEVICE

CIRCUFLOW 5200 SEQUENTIAL COMPRESSION DEVICE is an FDA 510(k)-cleared medical device (K101523) manufactured by Devon Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 16, 2010. Regulation: 8.