510(k) K050756 ยท DQX Wire, Guide, Catheter
SKIPPER AND SKIPPER RACE GUIDEWIRE
| Applicant | Invatec Innovative Technologies, S.R.L., Plymouth MN, US |
| Decision | Substantially Equivalent, May 5, 2005 |
| Received | Mar 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050756
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.