K233532
- 510(k) number
- K233532
- Device name
- MULTIX Impact E
- Applicant
- Siemens Medical Solutions PA · US
- Product code
- KPR — System, X-Ray, Stationary
- Decision date
- 2023-11-29
- Date received
- 2023-11-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K233532.pdf
Official FDA record: K233532
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.