K-number	K240394
Device name	multiFlux 1000 (F00012408)
Applicant	Fresenius Medical Care Renal Therapies Group, LLC
Product code	KDI
Device class	Class II
Decision date	May 31, 2024
Decision	Substantially Equivalent
Regulation	876.5860

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Source

View the full FDA submission: accessdata.fda.gov

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multiFlux 1000 (F00012408)

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