510(k) K162384 ยท DQY Catheter, Percutaneous
TrailBlazer Angled Support Catheter
| Applicant | Medtronic Vascular, Inc.(Formerly Ev3 Inc.), Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 22, 2016 |
| Received | Aug 25, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162384
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.