K-number	K000921
Device name	BAYER ADVIA IMS SYSTEM; 200 + 3
Applicant	Bayer Corp.
Product code	DER
Device class	Class II
Decision date	May 18, 2000
Decision	Substantially Equivalent
Regulation	866.5580

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View the full FDA submission: accessdata.fda.gov

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BAYER ADVIA IMS SYSTEM; 200 + 3

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