K262120
- 510(k) number
- K262120
- Device name
- Avara Viewer
- Applicant
- Avara Software FL · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-07-10
- Date received
- 2026-06-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K262120.pdf
Official FDA record: K262120
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.