PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE

PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE is an FDA 510(k)-cleared medical device (K090286) manufactured by Advanced Vascular Dynamics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 2009. Regulation: 8.