FDA 510(k)

X-Clever（ASHK100G）

K号: K233599 · 2024-03-18

决定日期2024-03-18

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

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.

常见问题

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)记录显示LG Electronics.Inc为申请人。这本身并不能确立该设备的制造商。

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

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

列明Lg Electronics.Inc为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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