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FDA 510(k) Applications Submitted by Siemens Medical Soultions USA, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231351
05/09/2023
Chondral Quant
Siemens Medical Soultions USA, Inc.
K200515
03/02/2020
syngo.CT Cardiac Planning
Siemens Medical Soultions USA, Inc.
K191309
05/14/2019
syngo.via MI Workflows VB40A, Scenium
Siemens Medical Soultions USA, Inc.
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