510(k) K173614 ยท HCG Device, Neurovascular Embolization
Penumbra Coil 400, Ruby Coil System, POD System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Apr 17, 2018 |
| Received | Nov 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173614
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.