DRAGER OXYLOG 2000

DRAGER OXYLOG 2000 is an FDA 510(k)-cleared medical device (K984577) 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 January 21, 1999. Regulation: 8.