510(k) K821846 ยท DRX Electrode, Electrocardiograph
LDS MONITORING ELECTRODE
| Applicant | Life Design Systems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 30, 1982 |
| Received | Jun 22, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821846
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.