510(k) K813176 ยท DRX Electrode, Electrocardiograph
GEL ELECTRODE
| Applicant | Dyn-A-Med Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 29, 1981 |
| Received | Nov 12, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813176
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.