FORA P100 血压监测系统
K号: K182934 · 2019-02-12
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器械摘要
常见问题
What is the FORA P100 Blood Pressure Monitoring System?
FORA P100 Blood Pressure Monitoring System is a medical device that received FDA 510(k) clearance on 2019-02-12. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K182934.
When did FORA P100 Blood Pressure Monitoring System receive FDA 510(k) clearance?
FORA P100 Blood Pressure Monitoring System received FDA 510(k) clearance on 2019-02-12, under 510(k) number K182934.
Who is the listed applicant for FORA P100 Blood Pressure Monitoring System?
The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORA P100 Blood Pressure Monitoring System?
The FDA product code for FORA P100 Blood Pressure Monitoring System is DXN.
相关临床试验
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列明Taidoc Technology Corporation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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