510(k) K123765 ยท DQY Catheter, Percutaneous
GUIDEZILLA GUIDE EXTENSION CATHETER
| Applicant | Boston Scientific, Maple Grove MN, US |
| Decision | Substantially Equivalent, Mar 19, 2013 |
| Received | Dec 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123765
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.