qEEG-Pro
K 號：K171414 · 2018-07-01
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器材摘要
qEEG-Pro is the device name listed in this FDA 510(k) record. The listed applicant is Brainmaster Technologies, Inc.. It received FDA 510(k) clearance on 2018-07-01 under 510(k) number K171414. The device is classified under product code OLU. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the qEEG-Pro?
qEEG-Pro is a medical device that received FDA 510(k) clearance on 2018-07-01. The listed applicant is Brainmaster Technologies, Inc.. The 510(k) number is K171414.
When did qEEG-Pro receive FDA 510(k) clearance?
qEEG-Pro received FDA 510(k) clearance on 2018-07-01, under 510(k) number K171414.
Who is the listed applicant for qEEG-Pro?
The FDA 510(k) record lists Brainmaster Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for qEEG-Pro?
The FDA product code for qEEG-Pro is OLU.
其他以 Brainmaster Technologies, Inc. 為申請人之記錄
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相關器械（代碼：OLU）
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
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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