510(k) K915563 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
DIAGNOSTIC EP CATHETER
| Applicant | Arrhythmia Technologies, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Mar 9, 1992 |
| Received | Dec 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915563
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.