510(k) K083125 ยท DQY Catheter, Percutaneous
NEURON SELECT CATHETER SIZE 070
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Nov 21, 2008 |
| Received | Oct 22, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083125
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 8, 2009 | Penumbra Inc. Penumbra Neuron 5F Select Catheter, Neuro Deliver/Intracranial Access System Catheter, manufactured by Penumbra, Inc., Alameda, CA.
Intended for the introduction of interventional devices into the pe Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.