510(k) K113819 ยท DQO Catheter, Intravascular, Diagnostic
MONGOOSE ANGIOGRAPHIC CATHETER
| Applicant | Pediacath, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jul 11, 2012 |
| Received | Dec 27, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113819
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.