FDA 510(k)

27HJ713S

K 號：K170899 · 2017-05-30

決定日期2017-05-30

產品代碼GCJ

諮詢委員會GU

決定相當於

器材摘要

27HJ713S is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics. It received FDA 510(k) clearance on 2017-05-30 under 510(k) number K170899. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 27HJ713S?

27HJ713S is a medical device that received FDA 510(k) clearance on 2017-05-30. The listed applicant is Lg Electronics. The 510(k) number is K170899.

When did 27HJ713S receive FDA 510(k) clearance?

27HJ713S received FDA 510(k) clearance on 2017-05-30, under 510(k) number K170899.

Who is the listed applicant for 27HJ713S?

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

What is the FDA product code for 27HJ713S?

The FDA product code for 27HJ713S is GCJ.

其他以 Lg Electronics 為申請人之記錄

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相關器械（代碼：GCJ）

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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