510(k) K223615 ยท GWG Endoscope, Neurological
Digital ClarusScope System, Digital NeuroPEN System
| Applicant | Clarus Medical, LLC, Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 21, 2023 |
| Received | Dec 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223615
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.