510(k) K213390 ยท QJP Catheter, Percutaneous, Neurovasculature
Benchmark BMX96 Access System
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Aug 18, 2022 |
| Received | Oct 15, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213390
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.