510(k) K090554 ยท DQX Wire, Guide, Catheter
ACUITY MAILMAN AND STRAIT-TRAK GUIDEWIRE
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 2, 2009 |
| Received | Mar 2, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090554
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.