510(k) K191186 ยท GYC Electrode, Cortical
Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode
| Applicant | Ad-Tech Medical Instrument Corporation, Oak Creek WI, US |
| Decision | Substantially Equivalent, Jan 25, 2020 |
| Received | May 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191186
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.