电子血压计
K号: K222394 · 2023-03-03
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器械摘要
常见问题
What is the Electronic Sphygmomanometers?
Electronic Sphygmomanometers is a medical device that received FDA 510(k) clearance on 2023-03-03. The listed applicant is Qingdao Yasee Medical Device Co., Ltd.. The 510(k) number is K222394.
When did Electronic Sphygmomanometers receive FDA 510(k) clearance?
Electronic Sphygmomanometers received FDA 510(k) clearance on 2023-03-03, under 510(k) number K222394.
Who is the listed applicant for Electronic Sphygmomanometers?
The FDA 510(k) record lists Qingdao Yasee Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electronic Sphygmomanometers?
The FDA product code for Electronic Sphygmomanometers is DXN.
相关临床试验
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列明Qingdao Yasee Medical Device 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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