510(k) K141782 ยท DQX Wire, Guide, Catheter
HI-TORQUE VERSATURN GUIDE WIRE
| Applicant | Abbott Vascular, Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 7, 2014 |
| Received | Jul 2, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141782
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.