510(k) K142164 ยท LKF Cannula, Manipulator/Injector, Uterine
MANIPULATOR; MANIPULATOR PRO
| Applicant | Gynetech Pty. , Ltd., Pacifica CA, US |
| Decision | Substantially Equivalent, Dec 17, 2014 |
| Received | Aug 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142164
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.