Sourcerer
K 號：K241513 · 2024-09-27
廣告
決定日期2024-09-27
產品代碼OLX
諮詢委員會NE
(請提供完整的英文描述，以便進行翻譯。)
決定相當於
器材摘要
Sourcerer is the device name listed in this FDA 510(k) record. The listed applicant is Brain Electrophysiology Laboratory Company, LLC. It received FDA 510(k) clearance on 2024-09-27 under 510(k) number K241513. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Sourcerer?
Sourcerer is a medical device that received FDA 510(k) clearance on 2024-09-27. The listed applicant is Brain Electrophysiology Laboratory Company, LLC. The 510(k) number is K241513.
When did Sourcerer receive FDA 510(k) clearance?
Sourcerer received FDA 510(k) clearance on 2024-09-27, under 510(k) number K241513.
Who is the listed applicant for Sourcerer?
The FDA 510(k) record lists Brain Electrophysiology Laboratory Company, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sourcerer?
The FDA product code for Sourcerer is OLX.
相關臨床試驗
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其他以 Brain Electrophysiology Laboratory Company, LLC 為申請人之記錄
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。
相關器械（代碼：OLX）
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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