FDA 510(k)

eKuore Pro 系列

K 號：K203007 · 2020-10-30

決定日期2020-10-30

產品代碼DQD

諮詢委員會履歷

決定相當於

器材摘要

eKuore Pro Series is the device name listed in this FDA 510(k) record. The listed applicant is Chip Ideas Electronics S.L.. It received FDA 510(k) clearance on 2020-10-30 under 510(k) number K203007. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the eKuore Pro Series?

eKuore Pro Series is a medical device that received FDA 510(k) clearance on 2020-10-30. The listed applicant is Chip Ideas Electronics S.L.. The 510(k) number is K203007.

When did eKuore Pro Series receive FDA 510(k) clearance?

eKuore Pro Series received FDA 510(k) clearance on 2020-10-30, under 510(k) number K203007.

Who is the listed applicant for eKuore Pro Series?

The FDA 510(k) record lists Chip Ideas Electronics S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for eKuore Pro Series?

The FDA product code for eKuore Pro Series is DQD.

其他以 Chip Ideas Electronics S.L. 為申請人之記錄

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相關器械（代碼：DQD）

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