K-number	K191040
Device name	syngo.via (Version VB40A)
Applicant	Siemens Healthcare GmbH
Product code	LLZ
Device class	Class II
Decision date	May 16, 2019
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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syngo.via (Version VB40A)

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