自动腕带式蓝牙血压计
K号: K170545 · 2017-11-21
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器械摘要
常见问题
What is the Automatic Wrist Bluetooth Blood Pressure Monitor?
Automatic Wrist Bluetooth Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2017-11-21. The listed applicant is Truly Instrument , Ltd.. The 510(k) number is K170545.
When did Automatic Wrist Bluetooth Blood Pressure Monitor receive FDA 510(k) clearance?
Automatic Wrist Bluetooth Blood Pressure Monitor received FDA 510(k) clearance on 2017-11-21, under 510(k) number K170545.
Who is the listed applicant for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA 510(k) record lists Truly Instrument , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA product code for Automatic Wrist Bluetooth 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。
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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