510(k) K875041 ยท DRX Electrode, Electrocardiograph
FOAM BORDERED DIAGNOSTIC (CARE) ELECTRODE
| Applicant | Labeltape Meditect, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Jan 28, 1988 |
| Received | Dec 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875041
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.