510(k) K890705 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
MEDIMOD(TM), MODEL 8900
| Applicant | Medical Devices, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Mar 9, 1989 |
| Received | Feb 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890705
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.