510(k) K964272 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
PERFORMR SERIES EP DIAGNOSTIC CATHETERS
| Applicant | Medtronic Cardiorhythm, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jan 23, 1997 |
| Received | Oct 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964272
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.