icobrain ARIA
K号: K240712 · 2024-11-07
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器械摘要
icobrain aria is the device name listed in this FDA 510(k) record. The listed applicant is Icometrix NV. It received FDA 510(k) clearance on 2024-11-07 under 510(k) number K240712. The device is classified under product code QBS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the icobrain aria?
icobrain aria is a medical device that received FDA 510(k) clearance on 2024-11-07. The listed applicant is Icometrix NV. The 510(k) number is K240712.
When did icobrain aria receive FDA 510(k) clearance?
icobrain aria received FDA 510(k) clearance on 2024-11-07, under 510(k) number K240712.
Who is the listed applicant for icobrain aria?
The FDA 510(k) record lists Icometrix NV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for icobrain aria?
The FDA product code for icobrain aria is QBS.
相关临床试验
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列明Icometrix NV为申报人的其他记录
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相关器械（代码：QBS）
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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