FDA 510(k)

神經帽

K 號：K172866 · 2018-04-27

決定日期2018-04-27

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

NeuroCap is the device name listed in this FDA 510(k) record. The listed applicant is Memory MD, Inc.. It received FDA 510(k) clearance on 2018-04-27 under 510(k) number K172866. 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 NeuroCap?

NeuroCap is a medical device that received FDA 510(k) clearance on 2018-04-27. The listed applicant is Memory MD, Inc.. The 510(k) number is K172866.

When did NeuroCap receive FDA 510(k) clearance?

NeuroCap received FDA 510(k) clearance on 2018-04-27, under 510(k) number K172866.

Who is the listed applicant for NeuroCap?

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

What is the FDA product code for NeuroCap?

The FDA product code for NeuroCap is GXY.

其他以 Memory MD, 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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