510(k) K812878 ยท DRX Electrode, Electrocardiograph
THE NEW 1600 ELECTRODE
| Applicant | Andover Medical, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 2, 1981 |
| Received | Oct 14, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812878
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.