510(k) K181770 ยท LKF Cannula, Manipulator/Injector, Uterine
Intrauterine Access Balloon Catheter, Selective Salpingography Catheter
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Mar 29, 2019 |
| Received | Jul 3, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181770
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.