MeVis 肝脏套件
K号: K232045 · 2023-10-27
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器械摘要
MeVis Liver Suite is the device name listed in this FDA 510(k) record. The listed applicant is MeVis Medical Solutions AG. It received FDA 510(k) clearance on 2023-10-27 under 510(k) number K232045. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MeVis Liver Suite?
MeVis Liver Suite is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is MeVis Medical Solutions AG. The 510(k) number is K232045.
When did MeVis Liver Suite receive FDA 510(k) clearance?
MeVis Liver Suite received FDA 510(k) clearance on 2023-10-27, under 510(k) number K232045.
Who is the listed applicant for MeVis Liver Suite?
The FDA 510(k) record lists MeVis Medical Solutions AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MeVis Liver Suite?
The FDA product code for MeVis Liver Suite is JAK.
相关临床试验
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列明MeVis Medical Solutions AG为申报人的其他记录
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相关器械（代码：JAK）
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。
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官方来源
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