510(k) K970602 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
VAGINAL 2 ELECTRODE STIMULATION/EMG PROBE-SMALL
| Applicant | Hollister, Inc., Libertyville IL, US |
| Decision | Substantially Equivalent, Apr 15, 1997 |
| Received | Feb 18, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970602
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.