K240844
- 510(k) number
- K240844
- Device name
- Spectral CT 7500 RT
- Applicant
- Philips Medical Systems Technologies , Ltd. IL
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2024-10-18
- Date received
- 2024-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K240844.pdf
Official FDA record: K240844
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.