510(k) K151622 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
St.Jude Medical MediGuide Enabled Livewire Steerable Electrophysiology Catheter, Livewire Electrophysiology Catheter, Response Electrophysiology Catheter with Lumen, Response Electrophysiology Catheter and SJM Epicardial Catheter System, Supreme Electrophysiology Catheter
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Jul 15, 2015 |
| Received | Jun 16, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151622
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.