FDA 510(k) Applications Submitted by Shenzhen Konmed Technology Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K233576 11/07/2023 Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013; Rectal Probe: KM-502, KM-5018) Shenzhen Konmed Technology Co., Ltd.
K202648 09/11/2020 Biofeedback Nerve and Muscle Stimulator Shenzhen Konmed Technology Co., Ltd.
K163288 11/22/2016 Pelvifine Pelvic Muscle Trainer Shenzhen Konmed Technology Co., Ltd.


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