MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB is an FDA 510(k)-cleared medical device (K863581) manufactured by The Kendal Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 1986. Regulation: 8.