Qualis(linofilcon A)柔軟(親水)每日佩戴隐形眼鏡
K 號:K213216 · 2022-01-18
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器材摘要
常見問題
What is the Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device that received FDA 510(k) clearance on 2022-01-18. The listed applicant is Unicon Optical Co., Ltd.. The 510(k) number is K213216.
When did Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens receive FDA 510(k) clearance?
Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens received FDA 510(k) clearance on 2022-01-18, under 510(k) number K213216.
Who is the listed applicant for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA 510(k) record lists Unicon Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens?
The FDA product code for Qualis (linofilcon A) Soft (Hydrophilic) Daily Wear Contact Lens is LPL.
相關臨床試驗
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其他以 Unicon Optical Co., Ltd. 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:LPL)
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。
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