510(k) K962009 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
UROSTYM
| Applicant | Laborie Medical Technologies, Ltd., South Burlington VT, US |
| Decision | Substantially Equivalent, May 20, 1997 |
| Received | May 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962009
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.