510(k) K932849 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
PMI TENS ELECTRODE
| Applicant | Pepin Mfg., Inc., Stoughton WI, US |
| Decision | Substantially Equivalent, Jan 27, 1994 |
| Received | Jun 10, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932849
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.