DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS

DRAGER VAPOR 19.1 ANESTHETIC VAPORIZERS is an FDA 510(k)-cleared medical device (K821650) 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 June 28, 1982. Regulation: 8.