510(k) K072012 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
REFLEXION SPIRAL VARIABLE RADIUS CATHETER
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Aug 22, 2007 |
| Received | Jul 23, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072012
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.