510(k) K251668 ยท QJP Catheter, Percutaneous, Neurovasculature
SurfRider 13 Microcatheter
| Applicant | Kaneka Americas Holding, Inc., Newark CA, US |
| Decision | Substantially Equivalent, Jan 5, 2026 |
| Received | May 30, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251668
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.