510(k) K223666 · MTD Catheter, Intracardiac Mapping, High-Density Array
Ablacath Mapping Catheter
| Applicant | Ablacon, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Mar 17, 2023 |
| Received | Dec 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223666
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.