510(k) K182315 ยท DQX Wire, Guide, Catheter
Magic Torque DLVR Guidewire
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Sep 26, 2018 |
| Received | Aug 27, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182315
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.