510(k) K232542 ยท QJP Catheter, Percutaneous, Neurovasculature
Wedge XL Delivery Catheter
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, May 16, 2024 |
| Received | Aug 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232542
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.