510(k) K233619 ยท DXE Catheter, Embolectomy
Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters
| Applicant | Edwards Lifesciences, Irvine CA, US |
| Decision | Substantially Equivalent, May 20, 2024 |
| Received | Nov 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233619
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.