510(k) K090752 ยท NRY Catheter, Thrombus Retriever
PENUMBRA SYSTEM (PENNUMBRA REPERFUSION CATHETER 054), MODEL PSC054; (PENUMBRA SEPARATOR 054), MODEL PSS054
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Sep 21, 2009 |
| Received | Mar 20, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090752
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.