510(k) K960496 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
LIBERTY LITE PFS SYSTEM
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Jun 27, 1996 |
| Received | Feb 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960496
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.