K-number	K223656
Device name	AmeriWater MediQA Reverse Osmosis System (MSP3HF)
Applicant	AmeriWater, LLC
Product code	FIP
Device class	Class II
Decision date	Feb 13, 2023
Decision	Substantially Equivalent
Regulation	876.5665

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View the full FDA submission: accessdata.fda.gov

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AmeriWater MediQA Reverse Osmosis System (MSP3HF)

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