510(k) K140557 ยท DQY Catheter, Percutaneous
MIVI 6F GUIDE CATHETER
| Applicant | Mivi, LLC, Maple Grove MN, US |
| Decision | Substantially Equivalent, Sep 18, 2014 |
| Received | Mar 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140557
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.