K252238
- 510(k) number
- K252238
- Device name
- CoroFlow Cardiovascular System
- Applicant
- Coroventis Research AB SE
- Product code
- DQK — Computer, Diagnostic, Programmable
- Decision date
- 2025-10-24
- Date received
- 2025-07-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K252238.pdf
Official FDA record: K252238
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.