Jmoon FlexGlow 光疗设备(JD20U SP,JD20U SG)
K号: K251825 · 2025-10-01
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器械摘要
常见问题
What is the Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?
Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is a medical device that received FDA 510(k) clearance on 2025-10-01. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. The 510(k) number is K251825.
When did Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) receive FDA 510(k) clearance?
Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) received FDA 510(k) clearance on 2025-10-01, under 510(k) number K251825.
Who is the listed applicant for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?
The FDA 510(k) record lists Shenzhen Ulike Smart Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?
The FDA product code for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is OHS.
相关临床试验
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列明Shenzhen Ulike Smart Electronics 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。
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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