K-number	K103220
Device name	VOYAGER PERITONEAL DIALYSIS SYSTEM
Applicant	Deka Research & Development Corp.
Product code	FKX
Device class	Class II
Decision date	Jul 29, 2011
Decision	Substantially Equivalent
Regulation	876.5630

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View the full FDA submission: accessdata.fda.gov

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VOYAGER PERITONEAL DIALYSIS SYSTEM

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