510(k) K941911 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
INNOVA PELVIC FLOOR STIMULATION SYSTEM
| Applicant | Empi, Arden Hills MN, US |
| Decision | Substantially Equivalent, Jan 20, 1995 |
| Received | Apr 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941911
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.