510(k) K113163 ยท NRY Catheter, Thrombus Retriever
PENUMBRA SYSTEM MAX
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Nov 23, 2011 |
| Received | Oct 26, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113163
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.