MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V

MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V is an FDA 510(k)-cleared medical device (K033657) manufactured by Living Data Technologies Corporation. 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 18, 2003. Regulation: 8.