ALLONUS Tech 假肢
K 號：K241616 · 2024-12-17
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器材摘要
ALLONUS Tech Prosthetics is the device name listed in this FDA 510(k) record. The listed applicant is Allonus Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-12-17 under 510(k) number K241616. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ALLONUS Tech Prosthetics?
ALLONUS Tech Prosthetics is a medical device that received FDA 510(k) clearance on 2024-12-17. The listed applicant is Allonus Tech Co., Ltd.. The 510(k) number is K241616.
When did ALLONUS Tech Prosthetics receive FDA 510(k) clearance?
ALLONUS Tech Prosthetics received FDA 510(k) clearance on 2024-12-17, under 510(k) number K241616.
Who is the listed applicant for ALLONUS Tech Prosthetics?
The FDA 510(k) record lists Allonus Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLONUS Tech Prosthetics?
The FDA product code for ALLONUS Tech Prosthetics is NHA.
相關臨床試驗
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相關器械（代碼：NHA）
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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