MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW

MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW is an FDA 510(k)-cleared medical device (K922669) manufactured by Koven and Assoc., 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 28, 1993. Regulation: 8.