510(k) K953185 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
PLATINUM SERIES EP DIAGNOSTIC CATHETERS
| Applicant | Medtronic Cardiorhythm, San Jose CA, US |
| Decision | Substantially Equivalent, Apr 15, 1996 |
| Received | Jul 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953185
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.