MissLan® 数字早孕快速测试
K号: K222305 · 2022-11-30
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器械摘要
常见问题
What is the MissLan™ Digital Pregnancy Rapid Test?
MissLan™ Digital Pregnancy Rapid Test is a medical device that received FDA 510(k) clearance on 2022-11-30. The listed applicant is Guangzhou Decheng Biotechnology Co., Ltd.. The 510(k) number is K222305.
When did MissLan™ Digital Pregnancy Rapid Test receive FDA 510(k) clearance?
MissLan™ Digital Pregnancy Rapid Test received FDA 510(k) clearance on 2022-11-30, under 510(k) number K222305.
Who is the listed applicant for MissLan™ Digital Pregnancy Rapid Test?
The FDA 510(k) record lists Guangzhou Decheng Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MissLan™ Digital Pregnancy Rapid Test?
The FDA product code for MissLan™ Digital Pregnancy Rapid Test is LCX.
相关临床试验
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列明Guangzhou Decheng Biotechnology 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:LCX)
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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