510(k) K060449 ยท DQX Wire, Guide, Catheter
HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE
| Applicant | Guidant Corporation, Temecula CA, US |
| Decision | Substantially Equivalent, May 30, 2006 |
| Received | Feb 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060449
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.