非侵入性血流动力学血压监测仪
K号: K190893 · 2019-08-07
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器械摘要
常见问题
What is the Non-invasive Hemodynamic Blood Pressure Monitor?
Non-invasive Hemodynamic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-08-07. The listed applicant is Vita-Course Technologies Co., Ltd.. The 510(k) number is K190893.
When did Non-invasive Hemodynamic Blood Pressure Monitor receive FDA 510(k) clearance?
Non-invasive Hemodynamic Blood Pressure Monitor received FDA 510(k) clearance on 2019-08-07, under 510(k) number K190893.
Who is the listed applicant for Non-invasive Hemodynamic Blood Pressure Monitor?
The FDA 510(k) record lists Vita-Course Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Non-invasive Hemodynamic Blood Pressure Monitor?
The FDA product code for Non-invasive Hemodynamic 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。
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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