510(k) K172846 ยท LKF Cannula, Manipulator/Injector, Uterine
Uterine Manipulator
| Applicant | Beijing Hangtian Kadi Technology R&D Institute, Beijing, CN |
| Decision | Substantially Equivalent, Jun 26, 2018 |
| Received | Sep 19, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172846
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.