510(k) K120330 ยท HCG Device, Neurovascular Embolization
PENUMBRA COIL SYSTEM/PENUMBRA COIL 400
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Apr 2, 2012 |
| Received | Feb 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120330
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.