510(k) K133317 ยท NRY Catheter, Thrombus Retriever
PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, May 13, 2014 |
| Received | Oct 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133317
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.