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FDA 510(k)

INNOLUX RIC

K 號：K162344 · 2016-12-20

申請人Innolux Corporation
決定日期2016-12-20
產品代碼MQB
諮詢委員會RA
決定相當於

器材摘要

INNOLUX RIC is the device name listed in this FDA 510(k) record. The listed applicant is Innolux Corporation. It received FDA 510(k) clearance on 2016-12-20 under 510(k) number K162344. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the INNOLUX RIC?

INNOLUX RIC is a medical device that received FDA 510(k) clearance on 2016-12-20. The listed applicant is Innolux Corporation. The 510(k) number is K162344.

When did INNOLUX RIC receive FDA 510(k) clearance?

INNOLUX RIC received FDA 510(k) clearance on 2016-12-20, under 510(k) number K162344.

Who is the listed applicant for INNOLUX RIC?

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

What is the FDA product code for INNOLUX RIC?

The FDA product code for INNOLUX RIC is MQB.

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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相關器械（代碼：MQB）

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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官方來源

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