FDA 510(k)

MHD TENS

K 號：K190115 · 2019-06-19

決定日期2019-06-19

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

MHD TENS is the device name listed in this FDA 510(k) record. The listed applicant is Minghuangda Electronic Co., Ltd.. It received FDA 510(k) clearance on 2019-06-19 under 510(k) number K190115. 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 MHD TENS?

MHD TENS is a medical device that received FDA 510(k) clearance on 2019-06-19. The listed applicant is Minghuangda Electronic Co., Ltd.. The 510(k) number is K190115.

When did MHD TENS receive FDA 510(k) clearance?

MHD TENS received FDA 510(k) clearance on 2019-06-19, under 510(k) number K190115.

Who is the listed applicant for MHD TENS?

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

What is the FDA product code for MHD TENS?

The FDA product code for MHD TENS is NUH.

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。

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