K-number	K781058
Device name	C-DAK 4000 ARTIFICIAL KIDNEY
Applicant	Cordis Corp.
Product code	FJI
Device class	Class II
Decision date	Aug 23, 1978
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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C-DAK 4000 ARTIFICIAL KIDNEY

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