DRAGER-VAPOR 19.3

DRAGER-VAPOR 19.3 is an FDA 510(k)-cleared medical device (K981773) manufactured by Draeger Medical, 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 July 5, 1998. Regulation: 8.