510(k) K802058 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
MAPPING PROBE MODEL #6540
| Applicant | Cardiac Pacemakers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 19, 1980 |
| Received | Aug 25, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802058
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.