应用生物系统™ 3500 Dx遗传分析仪和应用生物系统™ 3500xL Dx遗传分析仪
K号: K191030 · 2020-02-21
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器械摘要
常见问题
What is the Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?
Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer is a medical device that received FDA 510(k) clearance on 2020-02-21. The listed applicant is Life Technologies Corporation. The 510(k) number is K191030.
When did Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer receive FDA 510(k) clearance?
Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer received FDA 510(k) clearance on 2020-02-21, under 510(k) number K191030.
Who is the listed applicant for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?
The FDA 510(k) record lists Life Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer?
The FDA product code for Applied Biosystems™ 3500 Dx Genetic Analyzer and Applied Biosystems™ 3500xL Dx Genetic Analyzer is PCA.
相关临床试验
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。
列明Life Technologies Corporation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。
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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