reVive Light Therapy® 祛皱和痤疮LED设备
K号: K223482 · 2022-12-21
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器械摘要
常见问题
What is the reVive Light Therapy® Wrinkle and Acne LED Device?
reVive Light Therapy® Wrinkle and Acne LED Device is a medical device that received FDA 510(k) clearance on 2022-12-21. The listed applicant is Led Technologies, Inc.. The 510(k) number is K223482.
When did reVive Light Therapy® Wrinkle and Acne LED Device receive FDA 510(k) clearance?
reVive Light Therapy® Wrinkle and Acne LED Device received FDA 510(k) clearance on 2022-12-21, under 510(k) number K223482.
Who is the listed applicant for reVive Light Therapy® Wrinkle and Acne LED Device?
The FDA 510(k) record lists Led Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for reVive Light Therapy® Wrinkle and Acne LED Device?
The FDA product code for reVive Light Therapy® Wrinkle and Acne LED Device is OHS.
相关临床试验
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列明Led Technologies, 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。
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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