RIDGID VENA CAVA CANNULAE

RIDGID VENA CAVA CANNULAE is an FDA 510(k)-cleared medical device (K802543) manufactured by Texas Medical Products, 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 15, 1981. Regulation: 8.