K242925
- 510(k) number
- K242925
- Device name
- MR Contour DL
- Applicant
- GE Healthcare IL · US
- Product code
- QKB — Radiological Image Processing Software For Radiation
- Decision date
- 2025-04-01
- Date received
- 2024-09-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242925.pdf
Official FDA record: K242925
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.