K243005
- 510(k) number
- K243005
- Device name
- AudaxCeph Cephalogram Analysis Software
- Applicant
- Audax D.O.O. SI
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-05-30
- Date received
- 2024-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K243005.pdf
Official FDA record: K243005
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.