K-number	K231102
Device name	Symbia Pro.specta VA20A Family
Applicant	Siemens Medical Solutions USA, Inc.
Product code	KPS
Device class	Class II
Decision date	May 17, 2023
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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Symbia Pro.specta VA20A Family

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