510(k) K212505 ยท LKF Cannula, Manipulator/Injector, Uterine
DUMI ManipulatOR
| Applicant | The O R Company Pty, Ltd., Carrum Downs, AU |
| Decision | Substantially Equivalent, Jan 10, 2022 |
| Received | Aug 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212505
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.