K253520
- 510(k) number
- K253520
- Device name
- Photonova Spectra, Photonova Spectra Select
- Applicant
- Ge Medical Systems, LLC WI · US
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2026-03-20
- Date received
- 2025-11-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253520.pdf
Official FDA record: K253520
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.