510(k) K252317 ยท MOF Guide, Wire, Catheter, Neurovasculature
Zenith Micro Guidewire
| Applicant | Suzhou Zenith Vascular SciTech Limited, Suzhou, CN |
| Decision | Substantially Equivalent, Apr 16, 2026 |
| Received | Jul 25, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252317
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.