510(k) K954389 ยท DRX Electrode, Electrocardiograph
CONMED ECG/EKG ELECTRODES
| Applicant | Conmedcorp, Utica NY, US |
| Decision | Substantially Equivalent, May 16, 1996 |
| Received | Sep 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954389
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.