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K 號：K182967 · 2018-11-23
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器材摘要
Visor System is the device name listed in this FDA 510(k) record. The listed applicant is Cerebrotech Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-11-23 under 510(k) number K182967. The device is classified under product code QAF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Visor System?
Visor System is a medical device that received FDA 510(k) clearance on 2018-11-23. The listed applicant is Cerebrotech Medical Systems, Inc.. The 510(k) number is K182967.
When did Visor System receive FDA 510(k) clearance?
Visor System received FDA 510(k) clearance on 2018-11-23, under 510(k) number K182967.
Who is the listed applicant for Visor System?
The FDA 510(k) record lists Cerebrotech Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Visor System?
The FDA product code for Visor System is QAF.
相關臨床試驗
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相關器械（代碼：QAF）
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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