510(k) K201164 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Venus Viva MD Device
| Applicant | Venus Concept USA, Inc., Weston FL, US |
| Decision | Substantially Equivalent, Jun 26, 2020 |
| Received | May 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201164
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.