NeuroTrigger Basic (NTB)
K号: K223027 · 2023-10-10
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申请人Neurotrigger
决定日期2023-10-10
产品代码IPF
咨询委员会PM
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决定实质等同
器械摘要
NeuroTrigger Basic (NTB) is the device name listed in this FDA 510(k) record. The listed applicant is Neurotrigger. It received FDA 510(k) clearance on 2023-10-10 under 510(k) number K223027. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NeuroTrigger Basic (NTB)?
NeuroTrigger Basic (NTB) is a medical device that received FDA 510(k) clearance on 2023-10-10. The listed applicant is Neurotrigger. The 510(k) number is K223027.
When did NeuroTrigger Basic (NTB) receive FDA 510(k) clearance?
NeuroTrigger Basic (NTB) received FDA 510(k) clearance on 2023-10-10, under 510(k) number K223027.
Who is the listed applicant for NeuroTrigger Basic (NTB)?
The FDA 510(k) record lists Neurotrigger as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeuroTrigger Basic (NTB)?
The FDA product code for NeuroTrigger Basic (NTB) is IPF.
相关临床试验
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相关器械（代码：IPF）
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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