510(k) K011435 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
HMT 21, HMT 2000 URINARY INCONTINENCE SYSTEM
| Applicant | Hmt, Inc., Seoul, KR |
| Decision | Substantially Equivalent, Jun 22, 2001 |
| Received | May 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011435
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.