510(k) K940091 ยท HIR Perineometer
INNOVA VAGINAL EMG SENSING ELECTRODE
| Applicant | Empi, Arden Hills MN, US |
| Decision | Substantially Equivalent, Dec 29, 1994 |
| Received | Jan 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940091
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.