510(k) K213900 ยท GWQ Full-Montage Standard Electroencephalograph
WAVi SCAN EEG System and Accessories
| Applicant | Wavi Co., Denver CO, US |
| Decision | Substantially Equivalent, May 6, 2022 |
| Received | Dec 14, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213900
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.