K243186
- 510(k) number
- K243186
- Device name
- Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- KPS — System, Tomography, Computed, Emission
- Decision date
- 2024-10-30
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K243186.pdf
Official FDA record: K243186
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.