510(k) K913594 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
DYNEX IIIB, MODEL 89002026
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 23, 1991 |
| Received | Aug 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913594
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.