510(k) K251240 ยท QJP Catheter, Percutaneous, Neurovasculature
Branchor X Balloon Guide Catheter
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Jun 20, 2025 |
| Received | Apr 22, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251240
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.