510(k) K833251 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
MODEL MK II TENS
| Applicant | European Electronic Systems, Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Mar 5, 1984 |
| Received | Sep 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833251
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.