510(k) K171332 ยท GWG Endoscope, Neurological
Artemis Neuro Evacuation Device
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Aug 14, 2017 |
| Received | May 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171332
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.