FDA 510(k)

一次性膠粘表面電極，一次性/可重用杯形電極

K 號：K153019 · 2016-03-21

決定日期2016-03-21

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

Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Bio Protech, Inc.. It received FDA 510(k) clearance on 2016-03-21 under 510(k) number K153019. 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 Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes?

Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes is a medical device that received FDA 510(k) clearance on 2016-03-21. The listed applicant is Bio Protech, Inc.. The 510(k) number is K153019.

When did Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes receive FDA 510(k) clearance?

Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes received FDA 510(k) clearance on 2016-03-21, under 510(k) number K153019.

Who is the listed applicant for Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes?

The FDA 510(k) record lists Bio Protech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes?

The FDA product code for Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes is GXY.

其他以 Bio Protech, Inc. 為申請人之記錄

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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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