510(k) K031864 ยท DQX Wire, Guide, Catheter
NITREX NITINOL GUIDEWIRE
| Applicant | Ev3 Corporation, Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 24, 2003 |
| Received | Jun 16, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031864
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.