EOlife®
K 號：K221841 · 2023-03-18
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器材摘要
EOlife® is the device name listed in this FDA 510(k) record. The listed applicant is Archeon. It received FDA 510(k) clearance on 2023-03-18 under 510(k) number K221841. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the EOlife®?
EOlife® is a medical device that received FDA 510(k) clearance on 2023-03-18. The listed applicant is Archeon. The 510(k) number is K221841.
When did EOlife® receive FDA 510(k) clearance?
EOlife® received FDA 510(k) clearance on 2023-03-18, under 510(k) number K221841.
Who is the listed applicant for EOlife®?
The FDA 510(k) record lists Archeon as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EOlife®?
The FDA product code for EOlife® is BTM.
相關臨床試驗
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相關器械（代碼：BTM）
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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