510(k) K230284 ยท HCG Device, Neurovascular Embolization
Penumbra LP Coil System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Oct 25, 2023 |
| Received | Feb 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230284
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.