MindsEye 可扩展端口
K号: K202072 · 2020-08-26
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决定日期2020-08-26
产品代码GZT
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。
决定实质等同
器械摘要
MindsEye Expandable Port is the device name listed in this FDA 510(k) record. The listed applicant is Minnetronix Neuro, Inc.. It received FDA 510(k) clearance on 2020-08-26 under 510(k) number K202072. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MindsEye Expandable Port?
MindsEye Expandable Port is a medical device that received FDA 510(k) clearance on 2020-08-26. The listed applicant is Minnetronix Neuro, Inc.. The 510(k) number is K202072.
When did MindsEye Expandable Port receive FDA 510(k) clearance?
MindsEye Expandable Port received FDA 510(k) clearance on 2020-08-26, under 510(k) number K202072.
Who is the listed applicant for MindsEye Expandable Port?
The FDA 510(k) record lists Minnetronix Neuro, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MindsEye Expandable Port?
The FDA product code for MindsEye Expandable Port is GZT.
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相关器械（代码：GZT）
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
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