K-number	K233798
Device name	Moda-flx Hemodialysis System and Cartridge
Applicant	Diality, Inc.
Product code	KDI
Device class	Class II
Decision date	Aug 2, 2024
Decision	Substantially Equivalent
Regulation	876.5860

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View the full FDA submission: accessdata.fda.gov

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Moda-flx Hemodialysis System and Cartridge

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