510(k) K020180 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL
| Applicant | Woodside Biomedical, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Mar 21, 2002 |
| Received | Jan 18, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020180
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.