K241982
- 510(k) number
- K241982
- Device name
- DeepFoqus (DeepFoqus-Accelerate)
- Applicant
- Foqus Technologies, Inc. CA
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-04-04
- Date received
- 2024-07-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K241982.pdf
Official FDA record: K241982
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.