Trackit T4 脑电图放大器
K号: K172271 · 2018-05-04
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决定日期2018-05-04
产品代码GWQ
咨询委员会NE
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器械摘要
Trackit T4 EEG Amplifier is the device name listed in this FDA 510(k) record. The listed applicant is Lifelines , Ltd.. It received FDA 510(k) clearance on 2018-05-04 under 510(k) number K172271. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Trackit T4 EEG Amplifier?
Trackit T4 EEG Amplifier is a medical device that received FDA 510(k) clearance on 2018-05-04. The listed applicant is Lifelines , Ltd.. The 510(k) number is K172271.
When did Trackit T4 EEG Amplifier receive FDA 510(k) clearance?
Trackit T4 EEG Amplifier received FDA 510(k) clearance on 2018-05-04, under 510(k) number K172271.
Who is the listed applicant for Trackit T4 EEG Amplifier?
The FDA 510(k) record lists Lifelines , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trackit T4 EEG Amplifier?
The FDA product code for Trackit T4 EEG Amplifier is GWQ.
相关临床试验
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相关器械（代码：GWQ）
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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