510(k) K880492 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
INTERCEPT T.E.N.S. DEVICE
| Applicant | Medical Design & Manufacturing Corp., Westerville OH, US |
| Decision | Substantially Equivalent, Apr 18, 1988 |
| Received | Feb 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880492
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.