510(k) K203723 ยท QJP Catheter, Percutaneous, Neurovasculature
Branchor Balloon Guide Catheter
| Applicant | Asahi Intecc Co., Ltd., Seto, JP |
| Decision | Substantially Equivalent, Dec 10, 2021 |
| Received | Dec 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203723
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.