Cervello STIM
K 號：K151354 · 2016-01-27
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器材摘要
Cervello STIM is the device name listed in this FDA 510(k) record. The listed applicant is Blackrock Neuromed. It received FDA 510(k) clearance on 2016-01-27 under 510(k) number K151354. The device is classified under product code GYC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Cervello STIM?
Cervello STIM is a medical device that received FDA 510(k) clearance on 2016-01-27. The listed applicant is Blackrock Neuromed. The 510(k) number is K151354.
When did Cervello STIM receive FDA 510(k) clearance?
Cervello STIM received FDA 510(k) clearance on 2016-01-27, under 510(k) number K151354.
Who is the listed applicant for Cervello STIM?
The FDA 510(k) record lists Blackrock Neuromed as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cervello STIM?
The FDA product code for Cervello STIM is GYC.
相關臨床試驗
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相關器械（代碼：GYC）
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
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