510(k) K172393 ยท MTD Catheter, Intracardiac Mapping, High-Density Array
Advisor HD Grid Mapping Catheter, Sensor Enabled
| Applicant | St. Jude Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Apr 23, 2018 |
| Received | Aug 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172393
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.