K-number	K192921
Device name	Zeos Aqua Vision Pump and tube
Applicant	Hemodia Sas
Product code	HRX
Device class	Class II
Decision date	Oct 9, 2020
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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Zeos Aqua Vision Pump and tube

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