510(k) K152231 ยท DQX Wire, Guide, Catheter
Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Feb 12, 2016 |
| Received | Aug 7, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152231
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.