上臂血压计
K号: K193456 · 2020-07-16
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器械摘要
常见问题
What is the Arm Blood Pressure Monitor?
Arm Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-07-16. The listed applicant is Ningbo Ranor Medical Science & Technology Co., Ltd.. The 510(k) number is K193456.
When did Arm Blood Pressure Monitor receive FDA 510(k) clearance?
Arm Blood Pressure Monitor received FDA 510(k) clearance on 2020-07-16, under 510(k) number K193456.
Who is the listed applicant for Arm Blood Pressure Monitor?
The FDA 510(k) record lists Ningbo Ranor Medical Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Arm Blood Pressure Monitor?
The FDA product code for Arm 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Ningbo Ranor Medical Science & 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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