510(k) K163214 ยท LKF Cannula, Manipulator/Injector, Uterine
Unicare System, Unicare Manipulator
| Applicant | Clearpath Surgical, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Feb 7, 2017 |
| Received | Nov 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163214
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.