JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200

JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 is an FDA 510(k)-cleared medical device (K982136) manufactured by Schiff & Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 23, 1999. Regulation: 8.