K-number	K220281
Device name	multiFiltratePRO System
Applicant	Fresenius Medical Care Renal Therapies Group, LLC
Product code	KDI
Device class	Class II
Decision date	Dec 16, 2022
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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multiFiltratePRO System

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