510(k) K222690 ยท MOF Guide, Wire, Catheter, Neurovasculature
SmartGUIDE deflectable hydrophilic guidewire
| Applicant | Artiria Medical SA, Geneva, CH |
| Decision | Substantially Equivalent, Apr 24, 2023 |
| Received | Sep 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222690
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.