AGE 自动上臂血压计
K号: K153552 · 2016-06-01
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器械摘要
常见问题
What is the AGE Automatic Upper Arm Blood Pressure Monitor?
AGE Automatic Upper Arm Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2016-06-01. The listed applicant is Ageless Health Industrial Co., Ltd.. The 510(k) number is K153552.
When did AGE Automatic Upper Arm Blood Pressure Monitor receive FDA 510(k) clearance?
AGE Automatic Upper Arm Blood Pressure Monitor received FDA 510(k) clearance on 2016-06-01, under 510(k) number K153552.
Who is the listed applicant for AGE Automatic Upper Arm Blood Pressure Monitor?
The FDA 510(k) record lists Ageless Health Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AGE Automatic Upper Arm Blood Pressure Monitor?
The FDA product code for AGE Automatic Upper Arm Blood Pressure Monitor is DXN.
相关临床试验
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列明Ageless Health Industrial 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：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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