PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM

PROCORD MD3500 VASCULAR DIAGNOSTIC SYSTEM is an FDA 510(k)-cleared medical device (K896034) manufactured by D. E. Hokanson, 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 January 17, 1990. Regulation: 8.