510(k) K021436 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
TTECH MODEL 200E + TENS DEVICE
| Applicant | Theratech, Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Jul 30, 2002 |
| Received | May 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021436
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.