510(k) K001903 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
NEOCONTROL PELVIC FLOOR THERAPY SYSTEM
| Applicant | Neotonus, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Aug 29, 2000 |
| Received | Jun 22, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001903
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.