K-number	K864169
Device name	FRESENIUS HEMOFLOW F50 & F70
Applicant	Seratronics, Inc.
Product code	KDI
Device class	Class II
Decision date	Nov 6, 1986
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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FRESENIUS HEMOFLOW F50 & F70

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