K241837
- 510(k) number
- K241837
- Device name
- Limbus Contour
- Applicant
- Limbus Ai, Inc. CA
- Product code
- QKB — Radiological Image Processing Software For Radiation
- Decision date
- 2024-10-09
- Date received
- 2024-06-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K241837.pdf
Official FDA record: K241837
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.