510(k) K150519 ยท LKF Cannula, Manipulator/Injector, Uterine
ManipulatOR PRO, ManipulatOR
| Applicant | Gynetech Pty. , Ltd., Richmond, AU |
| Decision | Substantially Equivalent, Aug 19, 2015 |
| Received | Mar 2, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150519
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.