510(k) K823466 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
AUTO-TENS MODEL III DUAL CHANNEL REPLACE
| Applicant | Cbc Corp., Walker MI, US |
| Decision | Substantially Equivalent, Mar 7, 1983 |
| Received | Nov 19, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823466
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.