K250751
- 510(k) number
- K250751
- Device name
- DualView Catheter
- Applicant
- Terumo Corporation JP
- Product code
- DQO — Catheter, Intravascular, Diagnostic
- Decision date
- 2025-07-17
- Date received
- 2025-03-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K250751.pdf
Official FDA record: K250751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.