510(k) K801041 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)
3M R.F. CURRENT SUPPRESSOR
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, May 23, 1980 |
| Received | May 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801041
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.