VEA 对齐
K号: K231917 · 2024-01-05
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器械摘要
VEA Align is the device name listed in this FDA 510(k) record. The listed applicant is Eos Imaging. It received FDA 510(k) clearance on 2024-01-05 under 510(k) number K231917. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VEA Align?
VEA Align is a medical device that received FDA 510(k) clearance on 2024-01-05. The listed applicant is Eos Imaging. The 510(k) number is K231917.
When did VEA Align receive FDA 510(k) clearance?
VEA Align received FDA 510(k) clearance on 2024-01-05, under 510(k) number K231917.
Who is the listed applicant for VEA Align?
The FDA 510(k) record lists Eos Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEA Align?
The FDA product code for VEA Align is QIH.
相关临床试验
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列明Eos Imaging为申报人的其他记录
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相关器械（代码：QIH）
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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