FDA 510(k)经皮神经电刺激与经皮肌肉刺激(型号:SM9126)
K号: K220150 · 2022-02-17
决定日期2022-02-17
产品代码NUH
咨询委员会NE
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决定实质等同
器械摘要
TENS & PMS (Model: SM9126) is the device name listed in this FDA 510(k) record. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. It received FDA 510(k) clearance on 2022-02-17 under 510(k) number K220150. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TENS & PMS (Model: SM9126)?
TENS & PMS (Model: SM9126) is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. The 510(k) number is K220150.
When did TENS & PMS (Model: SM9126) receive FDA 510(k) clearance?
TENS & PMS (Model: SM9126) received FDA 510(k) clearance on 2022-02-17, under 510(k) number K220150.
Who is the listed applicant for TENS & PMS (Model: SM9126)?
The FDA 510(k) record lists Hong Qiangxing (Shenzhen) Electronics Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS & PMS (Model: SM9126)?
The FDA product code for TENS & PMS (Model: SM9126) is NUH.
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列明Hong Qiangxing (Shenzhen) Electronics Limited为申报人的其他记录
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