Elfor-L
K 號：K243852 · 2025-04-14
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器材摘要
Elfor-L is the device name listed in this FDA 510(k) record. The listed applicant is Elfi-Tech , Ltd.. It received FDA 510(k) clearance on 2025-04-14 under 510(k) number K243852. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Elfor-L?
Elfor-L is a medical device that received FDA 510(k) clearance on 2025-04-14. The listed applicant is Elfi-Tech , Ltd.. The 510(k) number is K243852.
When did Elfor-L receive FDA 510(k) clearance?
Elfor-L received FDA 510(k) clearance on 2025-04-14, under 510(k) number K243852.
Who is the listed applicant for Elfor-L?
The FDA 510(k) record lists Elfi-Tech , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Elfor-L?
The FDA product code for Elfor-L is DPW.
相關臨床試驗
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相關器械（代碼：DPW）
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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