510(k) K081803 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ST. JUDE MEDICAL EPICARDIAL CATHETER SYSTEM
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, May 13, 2009 |
| Received | Jun 26, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081803
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.