K-number	K122952
Device name	NIPRO PUREFLUX-L HEMODIALYZER
Applicant	Nipro Medical Corporation
Product code	FJI
Device class	Class II
Decision date	Dec 4, 2013
Decision	Substantially Equivalent
Regulation	876.5820

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Source

View the full FDA submission: accessdata.fda.gov

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NIPRO PUREFLUX-L HEMODIALYZER

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