CIONIC神經袖套（NS-200）
K 號：K243828 · 2025-05-02
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器材摘要
CIONIC NEURAL SLEEVE (NS-200) is the device name listed in this FDA 510(k) record. The listed applicant is Cionic, Inc.. It received FDA 510(k) clearance on 2025-05-02 under 510(k) number K243828. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CIONIC NEURAL SLEEVE (NS-200)?
CIONIC NEURAL SLEEVE (NS-200) is a medical device that received FDA 510(k) clearance on 2025-05-02. The listed applicant is Cionic, Inc.. The 510(k) number is K243828.
When did CIONIC NEURAL SLEEVE (NS-200) receive FDA 510(k) clearance?
CIONIC NEURAL SLEEVE (NS-200) received FDA 510(k) clearance on 2025-05-02, under 510(k) number K243828.
Who is the listed applicant for CIONIC NEURAL SLEEVE (NS-200)?
The FDA 510(k) record lists Cionic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIONIC NEURAL SLEEVE (NS-200)?
The FDA product code for CIONIC NEURAL SLEEVE (NS-200) is GZI.
相關臨床試驗
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相關器械（代碼：GZI）
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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