K-number	K801731
Device name	C-DAK DUO-FLUX ARTIFICIAL KIDNEY
Applicant	Cordis Corp.
Product code	KDI
Device class	Class II
Decision date	Aug 13, 1980
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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C-DAK DUO-FLUX ARTIFICIAL KIDNEY

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