K-number	K003425
Device name	CLIRANS E-SERIES HOLLOW FIBER DIALYZERS
Applicant	Terumo Medical Corp.
Product code	KDI
Device class	Class II
Decision date	Feb 1, 2001
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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CLIRANS E-SERIES HOLLOW FIBER DIALYZERS

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