510(k) K081021 ยท DQX Wire, Guide, Catheter
KINETIX GUIDEWIRE, PLUS GUIDEWIRE
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 8, 2008 |
| Received | Apr 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081021
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.