510(k) K902080 ยท DRX Electrode, Electrocardiograph
RED DOT 2269 INFANT MONITORING ELECTRODE
| Applicant | 3M Company, Cottae Grove MN, US |
| Decision | Substantially Equivalent, Jul 18, 1990 |
| Received | May 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902080
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.