510(k) K232321 · DRA Catheter, Steerable
FlexCath Contour Steerable Sheath
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Oct 31, 2023 |
| Received | Aug 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232321
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.