510(k) K072718 ยท NRY Catheter, Thrombus Retriever
PENUMBRA SYSTEM
| Applicant | Penumbra, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Dec 28, 2007 |
| Received | Sep 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072718
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 24, 2010 | Penumbra Inc. Penumbra System Reperfusion Catheter 032, catalog number PSC032, lot number lot F15020, manufactured by Penumbra, Alameda, CA. Terminated |
NRY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.