510(k) K083094 ยท DQX Wire, Guide, Catheter
STREAMER POLYMER GUIDEWIRE
| Applicant | Brivant, Ltd., Galway, IE |
| Decision | Substantially Equivalent, Jul 7, 2009 |
| Received | Oct 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083094
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.