510(k) K171604 · LKF Cannula, Manipulator/Injector, Uterine
Rösch Thurmond Fallopian Tube Catheterization Set, Fallopian Tube Catheterization Set, and Fallopian Tube Catheterization Wire Guide with Platinum Tip
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Feb 15, 2018 |
| Received | Jun 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171604
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.