電極片
K 號：K190700 · 2019-06-14
廣告
決定日期2019-06-14
產品代碼GXY
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
ELECTRODES PAD is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Bestpad Technology Development Co., Ltd.. It received FDA 510(k) clearance on 2019-06-14 under 510(k) number K190700. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ELECTRODES PAD?
ELECTRODES PAD is a medical device that received FDA 510(k) clearance on 2019-06-14. The listed applicant is Shenzhen Bestpad Technology Development Co., Ltd.. The 510(k) number is K190700.
When did ELECTRODES PAD receive FDA 510(k) clearance?
ELECTRODES PAD received FDA 510(k) clearance on 2019-06-14, under 510(k) number K190700.
Who is the listed applicant for ELECTRODES PAD?
The FDA 510(k) record lists Shenzhen Bestpad Technology Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRODES PAD?
The FDA product code for ELECTRODES PAD is GXY.
相關臨床試驗
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相關器械（代碼：GXY）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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