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FDA 510(k)

医用监护仪(21HQ613D)

K号: K240130 · 2024-02-15

决定日期2024-02-15
产品代码PGY
咨询委员会RA
决定实质等同

器械摘要

Medical Monitor (21HQ613D) 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 2024-02-15 under 510(k) number K240130. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Medical Monitor (21HQ613D)?

Medical Monitor (21HQ613D) is a medical device that received FDA 510(k) clearance on 2024-02-15. The listed applicant is Lg Electronics.Inc. The 510(k) number is K240130.

When did Medical Monitor (21HQ613D) receive FDA 510(k) clearance?

Medical Monitor (21HQ613D) received FDA 510(k) clearance on 2024-02-15, under 510(k) number K240130.

Who is the listed applicant for Medical Monitor (21HQ613D)?

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 Medical Monitor (21HQ613D)?

The FDA product code for Medical Monitor (21HQ613D) is PGY.

相关临床试验

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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。

查看所有 28 个设备 →

相关器械(代码:PGY)

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。

官方来源

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