510(k) K082290 ยท DQY Catheter, Percutaneous
NEURON DELIVERY CATHETER 070
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Oct 31, 2008 |
| Received | Aug 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082290
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 5, 2009 | Penumbra Inc. Penumbra Neuron Delivery Catheter 070, percutaneous catheter, catalog numbers PND6F0701058, PND6F070956, PND6F0701058M, and PND6F070956M; manufactured by Penumbra, Inc., Alameda, CA.
Indicated for t Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.