CRITERION, CRITERION I.V., MODIFIED

CRITERION, CRITERION I.V., MODIFIED is an FDA 510(k)-cleared medical device (K952267) manufactured by Nova-Ventrx. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 1, 1997. Regulation: 8.