510(k) K021359 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
DIGI-PRO TENS MODEL WL-2203 AND WL-2205
| Applicant | Well-Life Healthcare, Inc., Taichung, R.O.C., TW |
| Decision | Substantially Equivalent, Apr 30, 2002 |
| Received | Jan 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021359
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.