510(k) K890746 ยท BXN Stimulator, Nerve, Battery-Powered
MYOTEST DBS NERVE STIMULATOR
| Applicant | Biometer Intl. A/S, Denmark, DK |
| Decision | Substantially Equivalent, Jul 14, 1989 |
| Received | Feb 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890746
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.