510(k) K142321 ยท DQY Catheter, Percutaneous
Benchmark Intracranial Access System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jan 26, 2015 |
| Received | Aug 19, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142321
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.