510(k) K050371 ยท DQO Catheter, Intravascular, Diagnostic
MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER
| Applicant | Medrad, Inc., Indianola PA, US |
| Decision | Substantially Equivalent, Jun 7, 2005 |
| Received | Feb 14, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050371
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.