510(k) K904747 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
PEI PLAQUE ELECTRODE ARRAY
| Applicant | Prucka Engineering, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Oct 9, 1991 |
| Received | Oct 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904747
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.