510(k) K203521 ยท DQY Catheter, Percutaneous
FineCross M3
| Applicant | Ashitaka Factory of Terumo Corporation, Fujinomiya, JP |
| Decision | Substantially Equivalent, Mar 3, 2021 |
| Received | Dec 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203521
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.