510(k) K800758 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
TENZCARE DUAL-CHANNEL STIMULATOR
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Apr 10, 1980 |
| Received | Apr 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800758
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.