JOSTRA DUAL STAGE VENOUS RETURN CANNULAE

JOSTRA DUAL STAGE VENOUS RETURN CANNULAE is an FDA 510(k)-cleared medical device (K013944) manufactured by Jostra AG. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 2002. Regulation: 8.