VASO PRESS DVT SYSTEM, MODELS VP500, VP501

VASO PRESS DVT SYSTEM, MODELS VP500, VP501 is an FDA 510(k)-cleared medical device (K991038) manufactured by Britt Corp., 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 21, 2000. Regulation: 8.