510(k) K823583 ยท BXN Stimulator, Nerve, Battery-Powered
MYOTEST NERVE STIMULATOR
| Applicant | Prothia USA, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 30, 1982 |
| Received | Dec 6, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823583
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.