K253421
- 510(k) number
- K253421
- Device name
- Perfusion Measurement Platform v1
- Applicant
- Quantified Imaging Limited GB
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-06-22
- Date received
- 2025-10-01
- 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: K253421.pdf
Official FDA record: K253421
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.