510(k) K923916 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
VOYAGR SERIES DIAGNOSTIC EP CATHETERS
| Applicant | Cardiorhythm, San Jose CA, US |
| Decision | Substantially Equivalent, Feb 10, 1993 |
| Received | Jul 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923916
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.