Myolift QT
K 號：K213078 · 2023-04-27
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器材摘要
Myolift QT is the device name listed in this FDA 510(k) record. The listed applicant is Johari Digital Healthcare Limited. It received FDA 510(k) clearance on 2023-04-27 under 510(k) number K213078. 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 Myolift QT?
Myolift QT is a medical device that received FDA 510(k) clearance on 2023-04-27. The listed applicant is Johari Digital Healthcare Limited. The 510(k) number is K213078.
When did Myolift QT receive FDA 510(k) clearance?
Myolift QT received FDA 510(k) clearance on 2023-04-27, under 510(k) number K213078.
Who is the listed applicant for Myolift QT?
The FDA 510(k) record lists Johari Digital Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Myolift QT?
The FDA product code for Myolift QT is NFO.
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其他以 Johari Digital Healthcare Limited 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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