STOCKERT CENTRIFUGAL PUMP CONSOLE

STOCKERT CENTRIFUGAL PUMP CONSOLE is an FDA 510(k)-cleared medical device (K020571) manufactured by Stockert Instrumente GmbH. 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 22, 2002. Regulation: 8.