510(k) K233292 ยท GWF Stimulator, Electrical, Evoked Response
ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress
| Applicant | Inomed Medizintechnik GmbH, Emmendingen, DE |
| Decision | Substantially Equivalent, Oct 27, 2023 |
| Received | Sep 29, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233292
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.