510(k) K113498 ยท DQX Wire, Guide, Catheter
DISPOSABLE TORQUE DEVICE
| Applicant | Coeur, Inc., Lebanon TN, US |
| Decision | Substantially Equivalent, Jul 20, 2012 |
| Received | Nov 25, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113498
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.