K-number	K082414
Device name	OPTIFLUX F250NR, MODEL 0500325E
Applicant	Fresenius Medical Care North America
Product code	KDI
Device class	Class II
Decision date	Oct 28, 2008
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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OPTIFLUX F250NR, MODEL 0500325E

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