510(k) K002976 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
RESPONSE ELECTROPHYSIOLOGY CATHETER, SUPREME ELECTROPHYSIOLOGY CATHETER, MODEL 401XXX AND 401XXX
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Dec 22, 2000 |
| Received | Sep 25, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002976
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.