510(k) K931794 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
MARINR SERIES EP DIAGNOSTIC CATHETERS
| Applicant | Medtronic Cardiorhythm, San Jose CA, US |
| Decision | Substantially Equivalent, Jun 6, 1994 |
| Received | Apr 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931794
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.