510(k) K223432 ยท DQX Wire, Guide, Catheter
Vassallo GT 018 Hybrid
| Applicant | Filmecc Co., Ltd., Nagoya-Shi, JP |
| Decision | Substantially Equivalent, Mar 9, 2023 |
| Received | Nov 14, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223432
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.