510(k) K993721 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES
| Applicant | Laborie Medical Tech Corp., Williston VT, US |
| Decision | Substantially Equivalent, Nov 29, 1999 |
| Received | Nov 3, 1999 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K993721
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.