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FDA 510(k)

液晶顯示器(MD310C、MD310G、MD210G)

K 號:K170944 · 2017-05-25

決定日期2017-05-25
產品代碼PGY
諮詢委員會RA
決定相當於

器材摘要

LCD Monitor (MD310C, MD310G, MD210G) is the device name listed in this FDA 510(k) record. The listed applicant is Benq Corporation. It received FDA 510(k) clearance on 2017-05-25 under 510(k) number K170944. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LCD Monitor (MD310C, MD310G, MD210G)?

LCD Monitor (MD310C, MD310G, MD210G) is a medical device that received FDA 510(k) clearance on 2017-05-25. The listed applicant is Benq Corporation. The 510(k) number is K170944.

When did LCD Monitor (MD310C, MD310G, MD210G) receive FDA 510(k) clearance?

LCD Monitor (MD310C, MD310G, MD210G) received FDA 510(k) clearance on 2017-05-25, under 510(k) number K170944.

Who is the listed applicant for LCD Monitor (MD310C, MD310G, MD210G)?

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

What is the FDA product code for LCD Monitor (MD310C, MD310G, MD210G)?

The FDA product code for LCD Monitor (MD310C, MD310G, MD210G) is PGY.

相關臨床試驗

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相關器械(代碼:PGY)

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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