K231871
- 510(k) number
- K231871
- Device name
- Radify Triage
- Applicant
- Envisionit Deepai, Ltd. GB
- Product code
- QFM — Radiological Computer-Assisted Prioritization Softwa
- Decision date
- 2024-01-17
- Date received
- 2023-06-26
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231871.pdf
Official FDA record: K231871
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.