
Jostra AG
Free shipping on orders over $99 · 30-day returns
VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201 is an FDA 510(k)-cleared medical device (K003551) 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 July 10, 2001. Regulation: 8.