510(k) K201308 ยท GWG Endoscope, Neurological
Axonpen, Axonmonitor, Axonbox, Tablet
| Applicant | Clearmind Biomedical, Taipei, TW |
| Decision | Substantially Equivalent, Nov 27, 2020 |
| Received | May 15, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201308
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.