K-number	K232045
Device name	MeVis Liver Suite
Applicant	MeVis Medical Solutions AG
Product code	JAK
Device class	Class II
Decision date	Oct 27, 2023
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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MeVis Liver Suite

Everything you need for a 510(k) submission. Nothing you don't.