510(k) K093556 ยท LKF Cannula, Manipulator/Injector, Uterine
VCARE DX
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Mar 12, 2010 |
| Received | Nov 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093556
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.