510(k) K070331 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
UROSTYM BIOFEEDBACK AND STIMULATION DEVICE AND ACCESSORIES
| Applicant | Laborie Medical Technologies, Williston VT, US |
| Decision | Substantially Equivalent, May 4, 2007 |
| Received | Feb 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070331
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.