Oren LED 口周光疗系统
K号: K213024 · 2021-12-22
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器械摘要
常见问题
What is the Oren LED Perioral Light Therapy System?
Oren LED Perioral Light Therapy System is a medical device that received FDA 510(k) clearance on 2021-12-22. The listed applicant is Shenzhen Kaiyan Medical CO , Ltd.. The 510(k) number is K213024.
When did Oren LED Perioral Light Therapy System receive FDA 510(k) clearance?
Oren LED Perioral Light Therapy System received FDA 510(k) clearance on 2021-12-22, under 510(k) number K213024.
Who is the listed applicant for Oren LED Perioral Light Therapy System?
The FDA 510(k) record lists Shenzhen Kaiyan Medical CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oren LED Perioral Light Therapy System?
The FDA product code for Oren LED Perioral Light Therapy System is OHS.
相关临床试验
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列明Shenzhen Kaiyan Medical 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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