510(k) K241899 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Pelvic Floor Stimulator (Intrelief PFE)
| Applicant | Easymed Instruments Co., Ltd., Foshan, CN |
| Decision | Substantially Equivalent, Nov 27, 2024 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241899
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.