510(k) K123024 ยท DQX Wire, Guide, Catheter
TORQUE DEVICE
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 26, 2012 |
| Received | Sep 28, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123024
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.