510(k) K840646 ยท DRX Electrode, Electrocardiograph
CARDIOTRODE
| Applicant | Kholber Corp., Miami FL, US |
| Decision | Substantially Equivalent, Oct 26, 1984 |
| Received | Feb 15, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840646
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.