T.E.D. SEQUENTIAL COMPRESSION SLEEVES

T.E.D. SEQUENTIAL COMPRESSION SLEEVES is an FDA 510(k)-cleared medical device (K781357) manufactured by Kendall Research Center. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 1978. Regulation: 8.