FDA 510(k)

電子刺激器

K 號：K200354 · 2020-06-29

申請人Shenzhen Dongjilian Electronics Co., Ltd.

決定日期2020-06-29

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

Electronic stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. It received FDA 510(k) clearance on 2020-06-29 under 510(k) number K200354. 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 Electronic stimulator?

Electronic stimulator is a medical device that received FDA 510(k) clearance on 2020-06-29. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. The 510(k) number is K200354.

When did Electronic stimulator receive FDA 510(k) clearance?

Electronic stimulator received FDA 510(k) clearance on 2020-06-29, under 510(k) number K200354.

Who is the listed applicant for Electronic stimulator?

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

What is the FDA product code for Electronic stimulator?

The FDA product code for Electronic stimulator is NUH.

其他以 Shenzhen Dongjilian Electronics Co., Ltd. 為申請人之記錄

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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。

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官方來源

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