510(k) K091825 ยท DQX Wire, Guide, Catheter
HI-TORQUE PROGRESS GUIDE WIRE FAMILY
| Applicant | Abbott Vascular, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, Sep 25, 2009 |
| Received | Jun 19, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091825
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.