K243350
- 510(k) number
- K243350
- Device name
- Rapid Neuro3D
- Applicant
- Ischemaview, Inc. CO · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-01-22
- Date received
- 2024-10-28
- 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: K243350.pdf
Official FDA record: K243350
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.