K243548
- 510(k) number
- K243548
- Device name
- BriefCase-Triage
- Applicant
- Aidoc Medical , Ltd. IL
- Product code
- QFM — Radiological Computer-Assisted Prioritization Softwa
- Decision date
- 2024-12-11
- Date received
- 2024-11-15
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K243548.pdf
Official FDA record: K243548
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.