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FDA 510(k)

WAVi™ 耳機和 WAVi™ eSoc™ 一次性電極接觸

K 號：K162460 · 2017-04-28

申請人Wavi Co.
決定日期2017-04-28
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

WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts is the device name listed in this FDA 510(k) record. The listed applicant is Wavi Co.. It received FDA 510(k) clearance on 2017-04-28 under 510(k) number K162460. 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 WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts?

WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts is a medical device that received FDA 510(k) clearance on 2017-04-28. The listed applicant is Wavi Co.. The 510(k) number is K162460.

When did WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts receive FDA 510(k) clearance?

WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts received FDA 510(k) clearance on 2017-04-28, under 510(k) number K162460.

Who is the listed applicant for WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts?

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

What is the FDA product code for WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts?

The FDA product code for WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts is GXY.

相關臨床試驗

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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其他以 Wavi Co. 為申請人之記錄

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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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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