510(k) K993976 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR
| Applicant | The Prometheus Group, Duxbury MA, US |
| Decision | Substantially Equivalent, Feb 22, 2000 |
| Received | Nov 24, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993976
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.