K-number	K010793
Device name	OXYLOG 1000, MODEL 2M86840
Applicant	Drager Medizintechnik GmbH
Product code	CBK
Device class	Class II
Decision date	Dec 20, 2001
Decision	Substantially Equivalent
Regulation	868.5895

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View the full FDA submission: accessdata.fda.gov

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OXYLOG 1000, MODEL 2M86840

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