FURUI SHUNT, 2-WAY AND 3-WAY

FURUI SHUNT, 2-WAY AND 3-WAY is an FDA 510(k)-cleared medical device (K910004) manufactured by Theramed, 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 September 18, 1991. Regulation: 8.