510(k) K832516 ยท DRX Electrode, Electrocardiograph
MAGNATRODE CARDIAC MONITORING ELECTRODE
| Applicant | R2 Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 16, 1983 |
| Received | Jul 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832516
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.