神經軸 IB-Stim (01-1020)
K 號：K241533 · 2024-10-30
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器材摘要
NeurAxis IB-Stim (01-1020) is the device name listed in this FDA 510(k) record. The listed applicant is Neuraxis. It received FDA 510(k) clearance on 2024-10-30 under 510(k) number K241533. The device is classified under product code QHH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NeurAxis IB-Stim (01-1020)?
NeurAxis IB-Stim (01-1020) is a medical device that received FDA 510(k) clearance on 2024-10-30. The listed applicant is Neuraxis. The 510(k) number is K241533.
When did NeurAxis IB-Stim (01-1020) receive FDA 510(k) clearance?
NeurAxis IB-Stim (01-1020) received FDA 510(k) clearance on 2024-10-30, under 510(k) number K241533.
Who is the listed applicant for NeurAxis IB-Stim (01-1020)?
The FDA 510(k) record lists Neuraxis as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeurAxis IB-Stim (01-1020)?
The FDA product code for NeurAxis IB-Stim (01-1020) is QHH.
相關臨床試驗
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其他以 Neuraxis 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：QHH）
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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