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FDA 510(k)

ORA 方法 LED 刮痧 (GS-04)

K号: K252272 · 2025-10-09

决定日期2025-10-09
产品代码OHS
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

ORA Method LED Gua Sha (GS-04) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Kaiyan Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2025-10-09 under 510(k) number K252272. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ORA Method LED Gua Sha (GS-04)?

ORA Method LED Gua Sha (GS-04) is a medical device that received FDA 510(k) clearance on 2025-10-09. The listed applicant is Shenzhen Kaiyan Medical Equipment Co., Ltd.. The 510(k) number is K252272.

When did ORA Method LED Gua Sha (GS-04) receive FDA 510(k) clearance?

ORA Method LED Gua Sha (GS-04) received FDA 510(k) clearance on 2025-10-09, under 510(k) number K252272.

Who is the listed applicant for ORA Method LED Gua Sha (GS-04)?

FDA 510(k)记录将深圳凯研医疗设备有限公司列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for ORA Method LED Gua Sha (GS-04)?

The FDA product code for ORA Method LED Gua Sha (GS-04) is OHS.

相关临床试验

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列明Shenzhen Kaiyan Medical Equipment Co., Ltd.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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相关器械(代码:OHS)

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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