510(k) K241372 · MTD Catheter, Intracardiac Mapping, High-Density Array
Advisor HD Grid X Mapping Catheter, Sensor Enabled
| Applicant | ABBOTT MEDICAL, Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 9, 2024 |
| Received | May 15, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241372
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.