510(k) K150161 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Venus Viva SR Device
| Applicant | Venus Concept , Ltd., Sunrise FL, US |
| Decision | Substantially Equivalent, May 12, 2015 |
| Received | Jan 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150161
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.