K223754
- 510(k) number
- K223754
- Device name
- BraveCX
- Applicant
- Bering, Ltd. GB
- Product code
- QFM — Radiological Computer-Assisted Prioritization Softwa
- Decision date
- 2023-11-09
- Date received
- 2022-12-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K223754.pdf
Official FDA record: K223754
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.