510(k) K233959 ยท DYB Introducer, Catheter
EPi-Ease Epicardial Access Device (EAS)
| Applicant | AtriCure, Inc., Mason OH, US |
| Decision | Substantially Equivalent, Feb 13, 2024 |
| Received | Dec 15, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233959
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.