510(k) K232573 · DQO Catheter, Intravascular, Diagnostic
INFINITI Ambi Angiographic Catheter
| Applicant | Cordis US Corp, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Nov 21, 2023 |
| Received | Aug 25, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232573
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.