K232155
- 510(k) number
- K232155
- Device name
- syngo.CT Dual Energy
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2023-11-30
- Date received
- 2023-07-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232155.pdf
Official FDA record: K232155
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.