K250203
- 510(k) number
- K250203
- Device name
- SureAx-Guide
- Applicant
- Sureax Medical, LLC CA · US
- Product code
- DQX — Wire, Guide, Catheter
- Decision date
- 2025-10-17
- Date received
- 2025-01-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K250203.pdf
Official FDA record: K250203
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.