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FDA 510(k)

電擊治療與電動肌肉刺激器(MHD-1083)

K 號:K241678 · 2024-09-09

決定日期2024-09-09
產品代碼NUH
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

TENS & EMS Stimulator (MHD-1083) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Minghuangda Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-09-09 under 510(k) number K241678. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TENS & EMS Stimulator (MHD-1083)?

TENS & EMS Stimulator (MHD-1083) is a medical device that received FDA 510(k) clearance on 2024-09-09. The listed applicant is Shenzhen Minghuangda Electronics Co., Ltd.. The 510(k) number is K241678.

When did TENS & EMS Stimulator (MHD-1083) receive FDA 510(k) clearance?

TENS & EMS Stimulator (MHD-1083) received FDA 510(k) clearance on 2024-09-09, under 510(k) number K241678.

Who is the listed applicant for TENS & EMS Stimulator (MHD-1083)?

The FDA 510(k) record lists Shenzhen Minghuangda Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS & EMS Stimulator (MHD-1083)?

The FDA product code for TENS & EMS Stimulator (MHD-1083) is NUH.

相關臨床試驗

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相關器械(代碼:NUH)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

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