510(k) K222023 ยท DQY Catheter, Percutaneous
RayFlow
| Applicant | Hexacath, Rueil Malmaison, FR |
| Decision | Substantially Equivalent, Apr 6, 2023 |
| Received | Jul 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222023
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.