K-number	K220433
Device name	syngo Application Software (VE21)
Applicant	Siemens Medical Solution USA, Inc.
Product code	LLZ
Device class	Class II
Decision date	Aug 16, 2022
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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syngo Application Software (VE21)

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