醫用設備規範文本翻譯： Medi Lift PLUS
K 號：K220198 · 2023-06-28
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器材摘要
Medi Lift PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Ya-Man, Ltd.. It received FDA 510(k) clearance on 2023-06-28 under 510(k) number K220198. 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 Medi Lift PLUS?
Medi Lift PLUS is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Ya-Man, Ltd.. The 510(k) number is K220198.
When did Medi Lift PLUS receive FDA 510(k) clearance?
Medi Lift PLUS received FDA 510(k) clearance on 2023-06-28, under 510(k) number K220198.
Who is the listed applicant for Medi Lift PLUS?
The FDA 510(k) record lists Ya-Man, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medi Lift PLUS?
The FDA product code for Medi Lift PLUS is NFO.
其他以 Ya-Man, Ltd. 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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