David 家庭妊娠测试条,David 专业妊娠测试条
K号: K172627 · 2018-03-28
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器械摘要
常见问题
What is the David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette?
David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette is a medical device that received FDA 510(k) clearance on 2018-03-28. The listed applicant is Runbio Biotech Co.,Ltd. The 510(k) number is K172627.
When did David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette receive FDA 510(k) clearance?
David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette received FDA 510(k) clearance on 2018-03-28, under 510(k) number K172627.
Who is the listed applicant for David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette?
The FDA 510(k) record lists Runbio Biotech Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette?
The FDA product code for David Home Pregnancy Test Cassette, David Professional Pregnancy Test Cassette is LCX.
相关临床试验
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列明Runbio Biotech 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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