Neuro Assessment System NAS-1000
K号: K172892 · 2018-03-08
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决定日期2018-03-08
产品代码QBE
咨询委员会CV
请注意，由于原文未提供具体内容，以下是一个示例翻译：
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产品名称：[产品名称]
公司名称：[公司名称]
FDA批准号：[FDA批准号]
510(k)申请号：[510(k)申请号]
PMA申请号：[PMA申请号]
临床试验注册号：[NCT]
PubMed ID：[PMID]
产品标识符：[标识符]
产品URL：[URL]
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请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
决定实质等同
器械摘要
Neuro Assessment System NAS-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Headsense Medical, Inc.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) number K172892. The device is classified under product code QBE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Neuro Assessment System NAS-1000?
Neuro Assessment System NAS-1000 is a medical device that received FDA 510(k) clearance on 2018-03-08. The listed applicant is Headsense Medical, Inc.. The 510(k) number is K172892.
When did Neuro Assessment System NAS-1000 receive FDA 510(k) clearance?
Neuro Assessment System NAS-1000 received FDA 510(k) clearance on 2018-03-08, under 510(k) number K172892.
Who is the listed applicant for Neuro Assessment System NAS-1000?
The FDA 510(k) record lists Headsense Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neuro Assessment System NAS-1000?
The FDA product code for Neuro Assessment System NAS-1000 is QBE.
相关临床试验
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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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