510(k) K880426 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
ELECTROSTIMULATOR MODEL 808
| Applicant | Cornell Enterprises Co., Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 19, 1988 |
| Received | Feb 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880426
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.