紅色
K 號：K242304 · 2024-12-06
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器材摘要
RED is the device name listed in this FDA 510(k) record. The listed applicant is Neuraxis, Inc.. It received FDA 510(k) clearance on 2024-12-06 under 510(k) number K242304. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RED?
RED is a medical device that received FDA 510(k) clearance on 2024-12-06. The listed applicant is Neuraxis, Inc.. The 510(k) number is K242304.
When did RED receive FDA 510(k) clearance?
RED received FDA 510(k) clearance on 2024-12-06, under 510(k) number K242304.
Who is the listed applicant for RED?
The FDA 510(k) record lists Neuraxis, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RED?
The FDA product code for RED is KLA.
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相關器械（代碼：KLA）
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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