510(k) K970077 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
LIBERTY PLUS SYSTEM(PFS-300)/VAGINAL PROBE, LIBERTY PLUS(PFS-044)
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, May 23, 1997 |
| Received | Jan 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970077
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.