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FDA 510(k)

IQ科技

K 號:K170659 · 2017-05-26

決定日期2017-05-26
產品代碼NUH
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

IQ Technologies is the device name listed in this FDA 510(k) record. The listed applicant is Iq Technologies, Inc.. It received FDA 510(k) clearance on 2017-05-26 under 510(k) number K170659. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IQ Technologies?

IQ Technologies is a medical device that received FDA 510(k) clearance on 2017-05-26. The listed applicant is Iq Technologies, Inc.. The 510(k) number is K170659.

When did IQ Technologies receive FDA 510(k) clearance?

IQ Technologies received FDA 510(k) clearance on 2017-05-26, under 510(k) number K170659.

Who is the listed applicant for IQ Technologies?

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

What is the FDA product code for IQ Technologies?

The FDA product code for IQ Technologies is NUH.

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相關器械(代碼:NUH)

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。

官方來源

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