K-number	K210075
Device name	Vigilant Software Suite Vigilant Master Med
Applicant	Fresenius Kabi AG
Product code	PHC
Device class	Class II
Decision date	Mar 1, 2022
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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Vigilant Software Suite Vigilant Master Med