VENTVIEW, MODEL 8414095

VENTVIEW, MODEL 8414095 is an FDA 510(k)-cleared medical device (K012177) manufactured by Drager Medizintechnik GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 3, 2001. Regulation: 8.