Diatron Pictus 700 临床化学分析仪,Diatron ISE,Diatron 葡萄糖己糖激酶法
K号: K151487 · 2016-01-14
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器械摘要
常见问题
What is the Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method?
Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method is a medical device that received FDA 510(k) clearance on 2016-01-14. The listed applicant is Diatron U.S., Inc.. The 510(k) number is K151487.
When did Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method receive FDA 510(k) clearance?
Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method received FDA 510(k) clearance on 2016-01-14, under 510(k) number K151487.
Who is the listed applicant for Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method?
The FDA 510(k) record lists Diatron U.S., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method?
The FDA product code for Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method is CFR.
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。
相关器械(代码:CFR)
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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