K233226
- 510(k) number
- K233226
- Device name
- FlexView Diagnostic (v1.1.20)
- Applicant
- Radical Imaging, LLC MA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-01-17
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K233226.pdf
Official FDA record: K233226
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.