510(k) K183062 ยท DQX Wire, Guide, Catheter
ASAHI Silverway
| Applicant | Asahi Intecc Co., Ltd., Hagoya-Shi, JP |
| Decision | Substantially Equivalent, Jul 1, 2019 |
| Received | Nov 5, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183062
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.