K-number	K002277
Device name	FRESENIUS OPTIFLUX 200NR
Applicant	Fresenius Medical Care North America
Product code	KDI
Device class	Class II
Decision date	Aug 25, 2000
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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FRESENIUS OPTIFLUX 200NR

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