510(k) K212977 ยท DQO Catheter, Intravascular, Diagnostic
SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
| Applicant | Cordis Corporation, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 17, 2022 |
| Received | Sep 17, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212977
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.