K251240
- 510(k) number
- K251240
- Device name
- Branchor X Balloon Guide Catheter
- Applicant
- Asahi Intecc Co., Ltd. JP
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2025-06-20
- Date received
- 2025-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251240.pdf
Official FDA record: K251240
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.