510(k) K203533 ยท DQX Wire, Guide, Catheter
VASSALLO GT
| Applicant | Filmecc Co., Ltd., Hagoya-Shi, JP |
| Decision | Substantially Equivalent, Apr 21, 2021 |
| Received | Dec 2, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203533
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.