510(k) K190464 ยท NRY Catheter, Thrombus Retriever
Penumbra System 3D Revascularization Device
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Apr 26, 2019 |
| Received | Feb 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190464
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.