510(k) K180031 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Endopath Electrosurgery Probe Plus II
| Applicant | Ethicon Endo-Surgery, LLC, Guaynabo PR, US |
| Decision | Substantially Equivalent, May 7, 2018 |
| Received | Jan 4, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180031
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.