510(k) K780186 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
NEUROMOD STIMULATOR MODEL 3723
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Mar 2, 1978 |
| Received | Feb 6, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780186
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.