VEEGix 腦電圖系統
K 號：K240593 · 2024-08-23
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器材摘要
VEEGix EEG System is the device name listed in this FDA 510(k) record. The listed applicant is NeuroServo, Inc.. It received FDA 510(k) clearance on 2024-08-23 under 510(k) number K240593. 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 VEEGix EEG System?
VEEGix EEG System is a medical device that received FDA 510(k) clearance on 2024-08-23. The listed applicant is NeuroServo, Inc.. The 510(k) number is K240593.
When did VEEGix EEG System receive FDA 510(k) clearance?
VEEGix EEG System received FDA 510(k) clearance on 2024-08-23, under 510(k) number K240593.
Who is the listed applicant for VEEGix EEG System?
The FDA 510(k) record lists NeuroServo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEEGix EEG System?
The FDA product code for VEEGix EEG System 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。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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