510(k) K101623 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
INQUIRY AFOCUSII DIAGNOSTIC CATHETER
| Applicant | St Jude Medical, Irvine CA, US |
| Decision | Substantially Equivalent, Aug 13, 2010 |
| Received | Jun 9, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101623
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.