K-number	K781237
Device name	KIDNEY, ARTIFICIAL, C-DAK 2.0
Applicant	Cordis Corp.
Product code	DJC
Device class	Class II
Decision date	Aug 31, 1978
Decision	Substantially Equivalent
Regulation	862.3610

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View the full FDA submission: accessdata.fda.gov

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KIDNEY, ARTIFICIAL, C-DAK 2.0

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