K241490
- 510(k) number
- K241490
- Device name
- Contour+ (MVision AI Segmentation)
- Applicant
- Mvision AI OY FI
- Product code
- QKB — Radiological Image Processing Software For Radiation
- Decision date
- 2024-10-18
- Date received
- 2024-05-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K241490.pdf
Official FDA record: K241490
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.