K-number	K831175
Device name	FILTRYZER HOLLOW FIBER ARTIF. KIDNEY
Applicant	Erika, Inc.
Product code	KOC
Device class	Class II
Decision date	Jun 22, 1984
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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FILTRYZER HOLLOW FIBER ARTIF. KIDNEY

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