Desnuda Reflect
K号: K211998 · 2021-11-18
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决定日期2021-11-18
产品代码NUC
咨询委员会OB
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器械摘要
Desnuda Reflect is the device name listed in this FDA 510(k) record. The listed applicant is Good Clean Love, Inc.. It received FDA 510(k) clearance on 2021-11-18 under 510(k) number K211998. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Desnuda Reflect?
Desnuda Reflect is a medical device that received FDA 510(k) clearance on 2021-11-18. The listed applicant is Good Clean Love, Inc.. The 510(k) number is K211998.
When did Desnuda Reflect receive FDA 510(k) clearance?
Desnuda Reflect received FDA 510(k) clearance on 2021-11-18, under 510(k) number K211998.
Who is the listed applicant for Desnuda Reflect?
The FDA 510(k) record lists Good Clean Love, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Desnuda Reflect?
The FDA product code for Desnuda Reflect is NUC.
相关临床试验
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列明Good Clean Love, 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：NUC）
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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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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