K-number	K103832
Device name	PHOENIX HEMODIALYSIS DELIVERY SYSTEM
Applicant	Gambro Renal Products, Inc.
Product code	KDI
Device class	Class II
Decision date	May 20, 2011
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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PHOENIX HEMODIALYSIS DELIVERY SYSTEM

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