FDA 510(k)

ASHK100G

K 號：K191188 · 2019-05-30

決定日期2019-05-30

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

ASHK100G is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics. It received FDA 510(k) clearance on 2019-05-30 under 510(k) number K191188. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ASHK100G?

ASHK100G is a medical device that received FDA 510(k) clearance on 2019-05-30. The listed applicant is Lg Electronics. The 510(k) number is K191188.

When did ASHK100G receive FDA 510(k) clearance?

ASHK100G received FDA 510(k) clearance on 2019-05-30, under 510(k) number K191188.

Who is the listed applicant for ASHK100G?

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 ASHK100G?

The FDA product code for ASHK100G is LLZ.

其他以 Lg Electronics 為申請人之記錄

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相關器械（代碼：LLZ）

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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