K-number	K062090
Device name	PRISMA SYSTEM R03.10A
Applicant	Gambro Renal Products
Product code	KDI
Device class	Class II
Decision date	Oct 18, 2006
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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PRISMA SYSTEM R03.10A

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