Seca 医疗生命体征分析仪 535，Seca mVSA 535，Seca mVSA，Seca 535
K号: K192092 · 2020-01-23
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器械摘要
常见问题
What is the Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 is a medical device that received FDA 510(k) clearance on 2020-01-23. The listed applicant is Seca GmbH & Co. KG. The 510(k) number is K192092.
When did Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 receive FDA 510(k) clearance?
Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 received FDA 510(k) clearance on 2020-01-23, under 510(k) number K192092.
Who is the listed applicant for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
The FDA 510(k) record lists Seca GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
The FDA product code for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 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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