510(k) K911813 ยท FBM Cannula And Trocar, Suprapubic, Non-Disposable
ENTREE CANNULA
| Applicant | Core Dynamics, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Jul 19, 1991 |
| Received | Apr 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911813
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.