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K 號：K192572 · 2019-12-17
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：OLT）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
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