CNS Envision
K号: K192572 · 2019-12-17
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决定日期2019-12-17
产品代码OLT
咨询委员会NE
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器械摘要
CNS Envision is the device name listed in this FDA 510(k) record. The listed applicant is Moberg Research, Inc.. It received FDA 510(k) clearance on 2019-12-17 under 510(k) number K192572. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CNS Envision?
CNS Envision is a medical device that received FDA 510(k) clearance on 2019-12-17. The listed applicant is Moberg Research, Inc.. The 510(k) number is K192572.
When did CNS Envision receive FDA 510(k) clearance?
CNS Envision received FDA 510(k) clearance on 2019-12-17, under 510(k) number K192572.
Who is the listed applicant for CNS Envision?
The FDA 510(k) record lists Moberg Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CNS Envision?
The FDA product code for CNS Envision is OLT.
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相关器械（代码：OLT）
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官方来源
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