FDA 510(k)

X-Clever (ASHK100G)

K 號：K233599 · 2024-03-18

決定日期2024-03-18

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

X-Clever (ASHK100G) is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics.Inc. It received FDA 510(k) clearance on 2024-03-18 under 510(k) number K233599. 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 X-Clever (ASHK100G)?

X-Clever (ASHK100G) is a medical device that received FDA 510(k) clearance on 2024-03-18. The listed applicant is Lg Electronics.Inc. The 510(k) number is K233599.

When did X-Clever (ASHK100G) receive FDA 510(k) clearance?

X-Clever (ASHK100G) received FDA 510(k) clearance on 2024-03-18, under 510(k) number K233599.

Who is the listed applicant for X-Clever (ASHK100G)?

FDA 510(k) 記錄將 Lg Electronics.Inc 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for X-Clever (ASHK100G)?

The FDA product code for X-Clever (ASHK100G) is LLZ.

其他以 Lg Electronics.Inc 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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官方來源

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