510(k) K190719 ยท GWG Endoscope, Neurological
Artemis Eye System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Aug 30, 2019 |
| Received | Mar 20, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190719
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.