K242781
- 510(k) number
- K242781
- Device name
- cvi42 Software Application
- Applicant
- Circle Cardiovascular Imaging, Inc. CA
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-10-15
- Date received
- 2024-09-16
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242781.pdf
Official FDA record: K242781
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.