510(k) K222254 ยท MMX Device, Percutaneous Retrieval
Gunther Tulip Vena Cava Filter Retrieval Set
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, May 16, 2023 |
| Received | Jul 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222254
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.