510(k) K211741 ยท DQX Wire, Guide, Catheter
Pre-Formed Extra Support Guidewire
| Applicant | Lake Region Medical, Chaska MN, US |
| Decision | Substantially Equivalent, Nov 22, 2021 |
| Received | Jun 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211741
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.