K-number	K232953
Device name	AquaBplus; AquaB LITE
Applicant	Fresenius Medical Care Renal Therapies Group, LLC
Product code	FIP
Device class	Class II
Decision date	Jun 13, 2024
Decision	Substantially Equivalent
Regulation	876.5665

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Source

View the full FDA submission: accessdata.fda.gov

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AquaBplus; AquaB LITE

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