K-number	K870724
Device name	FRESENIUS HEMOFLOW F60 AND F80
Applicant	Seratronics, Inc.
Product code	KDI
Device class	Class II
Decision date	Apr 1, 1987
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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FRESENIUS HEMOFLOW F60 AND F80

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