510(k) K220202 ยท LKF Cannula, Manipulator/Injector, Uterine
Uterine ElevatOR PRO with OccludOR Balloon
| Applicant | The O R Company Pty, Ltd., Carrum Downs, AU |
| Decision | Substantially Equivalent, Mar 31, 2022 |
| Received | Jan 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220202
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.