510(k) K902943 ยท DQO Catheter, Intravascular, Diagnostic
RSI FEMORAL GUIDING CATHETER
| Applicant | Retroperfusion Systems, Inc., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Oct 3, 1990 |
| Received | Jul 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902943
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.