510(k) K895183 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
REBOX II (TENS)
| Applicant | Rebox (Uk) , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jan 19, 1990 |
| Received | Aug 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895183
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.