电子血压计
K号: K212171 · 2021-11-01
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器械摘要
常见问题
What is the Electronic Blood Pressure Monitor?
Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2021-11-01. The listed applicant is Dongguan Kangweile Electronic Technology Co., Ltd.. The 510(k) number is K212171.
When did Electronic Blood Pressure Monitor receive FDA 510(k) clearance?
Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2021-11-01, under 510(k) number K212171.
Who is the listed applicant for Electronic Blood Pressure Monitor?
The FDA 510(k) record lists Dongguan Kangweile Electronic Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electronic Blood Pressure Monitor?
The FDA product code for Electronic 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Dongguan Kangweile Electronic 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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