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Draeger Medical B.V.
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OXYLOG 2000 PLUS SYSTEM (MODEL 5705080), OXYLOG 2000 PLUS BASIC DEVICE (MODEL 5705082) is an FDA 510(k)-cleared medical device (K082600) manufactured by Draeger Medical B.V.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 25, 2008. Regulation: 8.