K262143
- 510(k) number
- K262143
- Device name
- ImageGrid StreamVue
- Applicant
- Candelis, Inc. CA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2026-07-23
- Date received
- 2026-06-25
- 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: K262143.pdf
Official FDA record: K262143
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.