510(k) K040345 ยท DQX Wire, Guide, Catheter
MODIFICATION TO NITREX NITINOL GUIDEWIRE
| Applicant | Ev3, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 2, 2004 |
| Received | Feb 12, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040345
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.