510(k) K965066 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ARRHYTHMIA MAPPING SYSTEM (8100/8300)
| Applicant | Cardiac Pathways Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 11, 1997 |
| Received | Dec 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965066
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.