510(k) K070970 ยท DQY Catheter, Percutaneous
NEURON SUPPORT CATHETER SYSTEM, MODEL 5F/6F
| Applicant | Penumbra, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Aug 17, 2007 |
| Received | Apr 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070970
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 24, 2009 | Penumbra Inc. Penumbra Neuron Delivery Catheter 053, 115 cm/12 cm-- MP, manufactured by Penumbra Inc., Alameda, CA
Percutaneous Catheter, indicated for the introduction of interventional devices into the periphera Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.