510(k) K233201 ยท QJP Catheter, Percutaneous, Neurovasculature
MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Mar 27, 2024 |
| Received | Sep 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233201
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.