K-number	K823288
Device name	AMICON DIAFILTERS 20 & 30 HEMOFILTERS
Applicant	Amicon, Inc.
Product code	KDI
Device class	Class II
Decision date	Dec 16, 1982
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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AMICON DIAFILTERS 20 & 30 HEMOFILTERS

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