510(k) K955847 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
GYRO TIP EP CATHETER
| Applicant | Cardiac Assist Devices, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Jan 29, 1997 |
| Received | Dec 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955847
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.