510(k) K896155 ยท DRX Electrode, Electrocardiograph
RED DOT CARDIAC SENSOR SYSTEM
| Applicant | 3M Company, Cottae Grove MN, US |
| Decision | Substantially Equivalent, Dec 13, 1989 |
| Received | Oct 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896155
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.