510(k) K182487 ยท DQY Catheter, Percutaneous
CerusEndo Microcatheter
| Applicant | Cerus Endovascular, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Jul 20, 2019 |
| Received | Sep 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182487
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.