510(k) K212838 ยท QJP Catheter, Percutaneous, Neurovasculature
Benchmark Intracranial Access System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, May 27, 2022 |
| Received | Sep 7, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212838
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.