510(k) K881832 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
DS-200 AND DS-400 T.E.N.S.
| Applicant | Delta Marketing, Inc., Muskogee OK, US |
| Decision | Substantially Equivalent, Jul 1, 1988 |
| Received | Apr 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881832
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.