森田神經袖
K 號：K233322 · 2024-06-21
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器材摘要
Mochida Nerve Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Mochida Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233322. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Mochida Nerve Cuff?
Mochida Nerve Cuff is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Mochida Pharmaceutical Co., Ltd.. The 510(k) number is K233322.
When did Mochida Nerve Cuff receive FDA 510(k) clearance?
Mochida Nerve Cuff received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233322.
Who is the listed applicant for Mochida Nerve Cuff?
The FDA 510(k) record lists Mochida Pharmaceutical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Mochida Nerve Cuff?
The FDA product code for Mochida Nerve Cuff is JXI.
相關臨床試驗
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：JXI）
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
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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