NuFACE® FIX+
K 號：K240564 · 2024-06-27
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器材摘要
NuFACE® FIX+ is the device name listed in this FDA 510(k) record. The listed applicant is Carol Cole Company Dba Nuface®. It received FDA 510(k) clearance on 2024-06-27 under 510(k) number K240564. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NuFACE® FIX+?
NuFACE® FIX+ is a medical device that received FDA 510(k) clearance on 2024-06-27. The listed applicant is Carol Cole Company Dba Nuface®. The 510(k) number is K240564.
When did NuFACE® FIX+ receive FDA 510(k) clearance?
NuFACE® FIX+ received FDA 510(k) clearance on 2024-06-27, under 510(k) number K240564.
Who is the listed applicant for NuFACE® FIX+?
The FDA 510(k) record lists Carol Cole Company Dba Nuface® as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NuFACE® FIX+?
The FDA product code for NuFACE® FIX+ is NFO.
相關臨床試驗
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其他以 Carol Cole Company Dba Nuface® 為申請人之記錄
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。
相關器械（代碼：NFO）
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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