510(k) K050248 ยท DRX Electrode, Electrocardiograph
ELECTRODE
| Applicant | Electramold, Louisville KY, US |
| Decision | Substantially Equivalent, May 25, 2005 |
| Received | Feb 3, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050248
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.