水银血压计；单患者使用的水银血压计
K号: K222652 · 2022-11-28
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器械摘要
常见问题
What is the Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Cardicare Company, Ltd.. The 510(k) number is K222652.
When did Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer receive FDA 510(k) clearance?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer received FDA 510(k) clearance on 2022-11-28, under 510(k) number K222652.
Who is the listed applicant for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA 510(k) record lists Cardicare Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is DXQ.
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。
相关器械（代码：DXQ）
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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