NuFACE FIX皮膚緊緻設備
K 號：K182424 · 2018-12-18
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器材摘要
NuFACE FIX Skin Toning Device 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 2018-12-18 under 510(k) number K182424. 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 Skin Toning Device?
NuFACE FIX Skin Toning Device is a medical device that received FDA 510(k) clearance on 2018-12-18. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K182424.
When did NuFACE FIX Skin Toning Device receive FDA 510(k) clearance?
NuFACE FIX Skin Toning Device received FDA 510(k) clearance on 2018-12-18, under 510(k) number K182424.
Who is the listed applicant for NuFACE FIX Skin Toning Device?
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 Skin Toning Device?
The FDA product code for NuFACE FIX Skin Toning Device is NFO.
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其他以 Carol Cole Company Dba Nuface 為申請人之記錄
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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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