510(k) K181257 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PlasmaBlade X 3.0S, PlasmaBlade X 4.0
| Applicant | Medtronic Advanced Energy, Portsmouth NH, US |
| Decision | Substantially Equivalent, Aug 2, 2018 |
| Received | May 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181257
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.