K232751
- 510(k) number
- K232751
- Device name
- BriefCase-Triage
- Applicant
- Aidoc Medical , Ltd. IL
- Product code
- QAS — Radiological Computer-Assisted Triage And Notificati
- Decision date
- 2023-10-30
- Date received
- 2023-09-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232751.pdf
Official FDA record: K232751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.