510(k) K243756 · MOF Guide, Wire, Catheter, Neurovasculature
0.014 Willow Guidewire
| Applicant | Arbor Endovascular, LLC, San Jose CA, US |
| Decision | Substantially Equivalent, Jul 17, 2025 |
| Received | Dec 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243756
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.