510(k) K083706 ยท DQX Wire, Guide, Catheter
HI-TORQUE VERSACORE GUIDE WIRE
| Applicant | Abbott Vascular, Santa Clara CA, US |
| Decision | Substantially Equivalent, Feb 6, 2009 |
| Received | Dec 15, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083706
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.