510(k) K111380 ยท DQY Catheter, Percutaneous
NEURON MAX SYSTEM
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jul 19, 2011 |
| Received | May 16, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111380
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.