510(k) K091780 ยท DQO Catheter, Intravascular, Diagnostic
GUIDED MEASUREMENT CATHETER (GMC)
| Applicant | Mediguide, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Oct 16, 2009 |
| Received | Jun 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091780
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.