510(k) K191528 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Venus Legacy Pro Device
| Applicant | Venus Concept USA, Inc., Weston FL, US |
| Decision | Substantially Equivalent, Sep 6, 2019 |
| Received | Jun 10, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191528
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.