BIVONA CARDEN INTERMITTENT JETTING DEVICE

BIVONA CARDEN INTERMITTENT JETTING DEVICE is an FDA 510(k)-cleared medical device (K895946) manufactured by Bivona Medical Technologies. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 1990. Regulation: 8.