510(k) K242612 ยท DTK Filter, Intravascular, Cardiovascular
Option ELITE Vena Cava Filter System (352506070E 352506100E)
| Applicant | Argon Medical Devices, Inc., Athens TX, US |
| Decision | Substantially Equivalent, Sep 10, 2024 |
| Received | Sep 3, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242612
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.