510(k) K143135 ยท DQX Wire, Guide, Catheter
Spring Coil Guidewire
| Applicant | Neometrics, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 20, 2015 |
| Received | Oct 31, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143135
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.