NeuroField 分析套件
K号: K240420 · 2024-09-20
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决定日期2024-09-20
产品代码OLU
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
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器械摘要
NeuroField Analysis Suite is the device name listed in this FDA 510(k) record. The listed applicant is Neurofield, Inc.. It received FDA 510(k) clearance on 2024-09-20 under 510(k) number K240420. The device is classified under product code OLU. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NeuroField Analysis Suite?
NeuroField Analysis Suite is a medical device that received FDA 510(k) clearance on 2024-09-20. The listed applicant is Neurofield, Inc.. The 510(k) number is K240420.
When did NeuroField Analysis Suite receive FDA 510(k) clearance?
NeuroField Analysis Suite received FDA 510(k) clearance on 2024-09-20, under 510(k) number K240420.
Who is the listed applicant for NeuroField Analysis Suite?
The FDA 510(k) record lists Neurofield, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeuroField Analysis Suite?
The FDA product code for NeuroField Analysis Suite is OLU.
相关临床试验
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列明Neurofield, Inc.为申报人的其他记录
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：OLU）
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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