PixoTest 血糖监测系统
K号: K163087 · 2017-11-02
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器械摘要
常见问题
What is the PixoTest Blood Glucose Monitoring System?
PixoTest Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-11-02. The listed applicant is Ixensor Company , Ltd.. The 510(k) number is K163087.
When did PixoTest Blood Glucose Monitoring System receive FDA 510(k) clearance?
PixoTest Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-11-02, under 510(k) number K163087.
Who is the listed applicant for PixoTest Blood Glucose Monitoring System?
The FDA 510(k) record lists Ixensor Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PixoTest Blood Glucose Monitoring System?
The FDA product code for PixoTest Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
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:NBW)
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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