510(k) K022380 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
LIVESIRE ELECTROPHYSIOLOGY CATHETER
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Oct 1, 2002 |
| Received | Jul 22, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022380
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.