510(k) K963729 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
SD-610M(ALSO KNOWN AS STANDARD TENS, SD-609M,SD-611M, GLC-I STANDARD)
| Applicant | Skylark Device Co., Ltd., Taipei, TW |
| Decision | Substantially Equivalent, Feb 13, 1997 |
| Received | Sep 16, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963729
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.