510(k) K233791 ยท MOF Guide, Wire, Catheter, Neurovasculature
Drivewire 24 Guidewire
| Applicant | Rapid-Medical , Ltd., Yokneam, IL |
| Decision | Substantially Equivalent, Jul 11, 2024 |
| Received | Nov 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233791
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.