K233677
- 510(k) number
- K233677
- Device name
- Biograph VK10
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- KPS — System, Tomography, Computed, Emission
- Decision date
- 2024-01-12
- Date received
- 2023-11-16
- 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: K233677.pdf
Official FDA record: K233677
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.