510(k) K193579 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PlasmaBlade X 3.0S LIGHT
| Applicant | Medtronic Navigation, Louisville CO, US |
| Decision | Substantially Equivalent, Mar 24, 2020 |
| Received | Dec 23, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193579
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.