510(k) K180726 ยท DQX Wire, Guide, Catheter
Savion DLVR Guidewire, Savion FLX Guidewire
| Applicant | Boston Scientific, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 18, 2018 |
| Received | Mar 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180726
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.