手臂式血压计,数字血压计-自动上臂式
K号: K181104 · 2018-08-29
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器械摘要
常见问题
What is the Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style?
Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style is a medical device that received FDA 510(k) clearance on 2018-08-29. The listed applicant is Shenzhen Combei Technology Co., Ltd.. The 510(k) number is K181104.
When did Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style receive FDA 510(k) clearance?
Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style received FDA 510(k) clearance on 2018-08-29, under 510(k) number K181104.
Who is the listed applicant for Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style?
The FDA 510(k) record lists Shenzhen Combei Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style?
The FDA product code for Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style 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Shenzhen Combei Technology 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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