510(k) K021952 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
HIVOX DREAMATE DM-800
| Applicant | Hivox Biotek, Inc., Hsin-Chu City, TW |
| Decision | Substantially Equivalent, May 2, 2003 |
| Received | Jun 13, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021952
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.