OXYLOG 1000, MODEL 2M86840

OXYLOG 1000, MODEL 2M86840 is an FDA 510(k)-cleared medical device (K010793) manufactured by Drager Medizintechnik GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2001. Regulation: 8.