KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE

KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE is an FDA 510(k)-cleared medical device (K932835) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 1993. Regulation: 8.