510(k) K132931 ยท GWG Endoscope, Neurological
APOLLO SYSTEM
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jan 17, 2014 |
| Received | Sep 18, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132931
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.