510(k) K871441 ยท DRX Electrode, Electrocardiograph
ELECTRODE RTE-3, CLIP-ON DIAGNOSTIC ELECTRODE
| Applicant | Nitto Denko America, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Aug 3, 1987 |
| Received | Apr 13, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871441
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.