510(k) K241784 · DQX Wire, Guide, Catheter
Arrow® Nitinol Wire
| Applicant | Teleflex Medical, Morrisville NC, US |
| Decision | Substantially Equivalent, Sep 18, 2024 |
| Received | Jun 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241784
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.