510(k) K971444 ยท DRX Electrode, Electrocardiograph
3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES
| Applicant | 3M Medical Products Group, St Paul MN, US |
| Decision | Substantially Equivalent, Jun 11, 1997 |
| Received | Apr 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971444
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.