K251306
- 510(k) number
- K251306
- Device name
- Seg Pro V3 (RT-300)
- Applicant
- Ever Fortune.Ai, Co., Ltd. TW
- Product code
- QKB — Radiological Image Processing Software For Radiation
- Decision date
- 2026-01-28
- Date received
- 2025-04-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251306.pdf
Official FDA record: K251306
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.