K-number	K920757
Device name	FILTRAL HEMODIALYZERS
Applicant	C.G.H. Medical, Inc.
Product code	KDI
Device class	Class II
Decision date	Aug 5, 1994
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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FILTRAL HEMODIALYZERS

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