K250766
- 510(k) number
- K250766
- Device name
- LungQ 4
- Applicant
- Thirona BV NL
- Product code
- JAK — System, X-Ray, Tomography, Computed
- Decision date
- 2025-10-02
- Date received
- 2025-03-13
- 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: K250766.pdf
Official FDA record: K250766
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.