腕式血压计，血压计
K号: K210768 · 2021-07-30
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器械摘要
常见问题
What is the Wrist Blood Pressure Monitor, Blood Pressure Monitor?
Wrist Blood Pressure Monitor, Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2021-07-30. The listed applicant is Andon Health Co, Ltd.. The 510(k) number is K210768.
When did Wrist Blood Pressure Monitor, Blood Pressure Monitor receive FDA 510(k) clearance?
Wrist Blood Pressure Monitor, Blood Pressure Monitor received FDA 510(k) clearance on 2021-07-30, under 510(k) number K210768.
Who is the listed applicant for Wrist Blood Pressure Monitor, Blood Pressure Monitor?
The FDA 510(k) record lists Andon Health Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wrist Blood Pressure Monitor, Blood Pressure Monitor?
The FDA product code for Wrist Blood Pressure Monitor, Blood Pressure Monitor is DXN.
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Andon Health 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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