EVITA 4 (8411900)

EVITA 4 (8411900) is an FDA 510(k)-cleared medical device (K980642) manufactured by Drager, Inc.. 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, 1998. Regulation: 8.