510(k) K030140 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
DUOMED, SERIES 500, (MODELS ID 500, FL 500)
| Applicant | Duomed, Inc., West Palm Beach FL, US |
| Decision | Substantially Equivalent, Mar 18, 2003 |
| Received | Jan 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030140
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.