510(k) K233637 ยท DQY Catheter, Percutaneous
Cordis BRITECROSS Support Catheter
| Applicant | Cordis US Corp, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jun 28, 2024 |
| Received | Nov 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233637
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.