K251987
- 510(k) number
- K251987
- Device name
- Rapid Aortic Measurements
- Applicant
- Ischemaview, Inc. CO · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-09-23
- Date received
- 2025-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251987.pdf
Official FDA record: K251987
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.