K233543
- 510(k) number
- K233543
- Device name
- YSIO X.pree
- Applicant
- Siemens Medical Solutions PA · US
- Product code
- KPR — System, X-Ray, Stationary
- Decision date
- 2024-05-21
- Date received
- 2023-11-03
- 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: K233543.pdf
Official FDA record: K233543
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.