K241112
- 510(k) number
- K241112
- Device name
- BriefCase-Quantification
- Applicant
- Aidoc Medical , Ltd. IL
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-05-15
- Date received
- 2024-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241112.pdf
Official FDA record: K241112
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.