Digital Automatic Blood Pressure Monitor MD36 Series
K号: K191593 · 2019-07-22
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器械摘要
常见问题
What is the Digital Automatic Blood Pressure Monitor MD36 Series?
Digital Automatic Blood Pressure Monitor MD36 Series is a medical device that received FDA 510(k) clearance on 2019-07-22. The listed applicant is Grandway Technology (Shenzhen) Limited. The 510(k) number is K191593.
When did Digital Automatic Blood Pressure Monitor MD36 Series receive FDA 510(k) clearance?
Digital Automatic Blood Pressure Monitor MD36 Series received FDA 510(k) clearance on 2019-07-22, under 510(k) number K191593.
Who is the listed applicant for Digital Automatic Blood Pressure Monitor MD36 Series?
The FDA 510(k) record lists Grandway Technology (Shenzhen) Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Digital Automatic Blood Pressure Monitor MD36 Series?
The FDA product code for Digital Automatic Blood Pressure Monitor MD36 Series is DXN.
相关临床试验
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列明Grandway Technology (Shenzhen) Limited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:DXN)
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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