K243038
- 510(k) number
- K243038
- Device name
- Salix Central
- Applicant
- Artrya Limited AU
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-03-27
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243038.pdf
Official FDA record: K243038
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.