K-number	K992399
Device name	ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM
Applicant	Bayer Corp.
Product code	CIX
Device class	Class II
Decision date	Sep 15, 1999
Decision	Substantially Equivalent
Regulation	862.1035

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View the full FDA submission: accessdata.fda.gov

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ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM

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