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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