510(k) K041762 ยท DQX Wire, Guide, Catheter
FINISHING WIRE SUPPORTRAK
| Applicant | Guidant Corporation, St Paul MN, US |
| Decision | Substantially Equivalent, Aug 6, 2004 |
| Received | Jun 30, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041762
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.