510(k) K182542 ยท GWF Stimulator, Electrical, Evoked Response
The EPAD 2 System
| Applicant | Safeop Surgical, Inc., Hunt Valley MD, US |
| Decision | Substantially Equivalent, Feb 22, 2019 |
| Received | Sep 17, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182542
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.