紅緯
K 號：K211234 · 2021-09-17
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器材摘要
RedEx is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Concepts, Ltd.. It received FDA 510(k) clearance on 2021-09-17 under 510(k) number K211234. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RedEx?
RedEx is a medical device that received FDA 510(k) clearance on 2021-09-17. The listed applicant is Advanced Surgical Concepts, Ltd.. The 510(k) number is K211234.
When did RedEx receive FDA 510(k) clearance?
RedEx received FDA 510(k) clearance on 2021-09-17, under 510(k) number K211234.
Who is the listed applicant for RedEx?
The FDA 510(k) record lists Advanced Surgical Concepts, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RedEx?
The FDA product code for RedEx is GCJ.
相關臨床試驗
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相關器械（代碼：GCJ）
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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