腕式电子血压计
K号: K193386 · 2021-01-27
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器械摘要
常见问题
What is the Wrist Electronic Sphygmomanometer?
Wrist Electronic Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2021-01-27. The listed applicant is Shenzhen Changkun Technology Co., Ltd.. The 510(k) number is K193386.
When did Wrist Electronic Sphygmomanometer receive FDA 510(k) clearance?
Wrist Electronic Sphygmomanometer received FDA 510(k) clearance on 2021-01-27, under 510(k) number K193386.
Who is the listed applicant for Wrist Electronic Sphygmomanometer?
The FDA 510(k) record lists Shenzhen Changkun Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wrist Electronic Sphygmomanometer?
The FDA product code for Wrist Electronic Sphygmomanometer 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 Changkun 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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