K253574
- 510(k) number
- K253574
- Device name
- SOMATOM X.cite; SOMATOM X.ceed
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2026-03-20
- Date received
- 2025-11-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253574.pdf
Official FDA record: K253574
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.