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FDA 510(k)

ApolloVue S100影像系統

K 號:K201552 · 2020-09-02

決定日期2020-09-02
產品代碼NQQ
諮詢委員會RA
決定相當於

器材摘要

ApolloVue S100 Image System is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Medical Optics, Ltd.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K201552. The device is classified under product code NQQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ApolloVue S100 Image System?

ApolloVue S100 Image System is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Apollo Medical Optics, Ltd.. The 510(k) number is K201552.

When did ApolloVue S100 Image System receive FDA 510(k) clearance?

ApolloVue S100 Image System received FDA 510(k) clearance on 2020-09-02, under 510(k) number K201552.

Who is the listed applicant for ApolloVue S100 Image System?

The FDA 510(k) record lists Apollo Medical Optics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ApolloVue S100 Image System?

The FDA product code for ApolloVue S100 Image System is NQQ.

相關臨床試驗

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相關器械(代碼:NQQ)

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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