510(k) K790850 ยท GXY Electrode, Cutaneous
T.E.N.S.* SINGLE-USE ELECTRODE
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, May 31, 1979 |
| Received | May 4, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790850
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.