510(k) K230631 · DYB Introducer, Catheter
Kodiak Dual Port Coaxial Introducer Kit
| Applicant | Argon Medical Devices, Athens TX, US |
| Decision | Substantially Equivalent, May 22, 2023 |
| Received | Mar 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230631
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.