510(k) K952688 ยท HIR Perineometer
INNOVA RECTAL OR SMALL VAGINAL EMG SENSING ELECTRODE
| Applicant | Empi, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 6, 1995 |
| Received | Jun 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952688
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.