FEMORAL ARTERY PRESSURE PAD/DISK

FEMORAL ARTERY PRESSURE PAD/DISK is an FDA 510(k)-cleared medical device (K914149) manufactured by Disco, 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 December 12, 1991. Regulation: 8.