510(k) K131781 ยท LKF Cannula, Manipulator/Injector, Uterine
CLEARVIEW TOTAL
| Applicant | Clinical Innovations, LLC, Murray UT, US |
| Decision | Substantially Equivalent, May 28, 2014 |
| Received | Jun 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131781
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 30, 2019 | Clinical Innovations, LLC Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* * *CLINICAL INNOVATIONS Manufacturer: Clinical Innovations, LLC* * *Reorder Number: UM750* Terminated |
LKF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.