视界体
K号: K222386 · 2023-02-24
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决定日期2023-02-24
产品代码NGX
咨询委员会PM
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决定实质等同
器械摘要
Visionbody is the device name listed in this FDA 510(k) record. The listed applicant is Vb Technologies AG. It received FDA 510(k) clearance on 2023-02-24 under 510(k) number K222386. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Visionbody?
Visionbody is a medical device that received FDA 510(k) clearance on 2023-02-24. The listed applicant is Vb Technologies AG. The 510(k) number is K222386.
When did Visionbody receive FDA 510(k) clearance?
Visionbody received FDA 510(k) clearance on 2023-02-24, under 510(k) number K222386.
Who is the listed applicant for Visionbody?
The FDA 510(k) record lists Vb Technologies AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Visionbody?
The FDA product code for Visionbody is NGX.
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：NGX）
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
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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