510(k) K891007 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
NONIMPLANTED ELECTRICAL CONTINENCE DEVICE
| Applicant | Tridak Division of Indicon, Inc., Williston VT, US |
| Decision | Substantially Equivalent, Jun 7, 1990 |
| Received | Feb 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891007
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.