510(k) K891773 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
MICROGYN II ELEC STIM DEVICE TREAT OF URIN INCONTI
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Aug 23, 1989 |
| Received | Mar 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891773
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.