ATC OPTION FOR EVITA 2 DURA AND EVITA 4

ATC OPTION FOR EVITA 2 DURA AND EVITA 4 is an FDA 510(k)-cleared medical device (K992608) 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 August 23, 1999. Regulation: 8.