510(k) K981642 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
STABLEMAPR STEERABLE INTRACARDIAC CATHETERS
| Applicant | Medtronic Cardiorhythm, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 5, 1998 |
| Received | May 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981642
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.