510(k) K150262 ยท DTK Filter, Intravascular, Cardiovascular
Crux Vena Cava Filter System, femoral; Crux Vena Cava Filter System, jugular
| Applicant | Volcano Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, Apr 3, 2015 |
| Received | Feb 4, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150262
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.