510(k) K811499 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
TENSMAX
| Applicant | Anritsu America Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 20, 1981 |
| Received | May 27, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811499
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.