510(k) K233576 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013; Rectal Probe: KM-502, KM-5018)
| Applicant | Shenzhen Konmed Technology Co., Ltd., Pingshan District, Shenzhen, CN |
| Decision | Substantially Equivalent, Feb 23, 2024 |
| Received | Nov 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233576
No recall in the FDA data names this 510(k).
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