510(k) K990456 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
ANAL 2 ELECTRODE STIMULATION/EMG PROBE - W/STOP
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Mar 25, 1999 |
| Received | Feb 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990456
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.