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FDA 510(k)

保仕亮(kalifilcon A)軟性(親水性)老花眼隐形眼鏡

K 號:K210975 · 2021-05-24

決定日期2021-05-24
產品代碼LPL
諮詢委員會此為醫療器材法規文本之翻譯。根據醫療法規翻譯政策,以下為繁體中文譯文: 本文件概述適用於醫療器材之監管架構,包括美國食品藥物管理局(FDA)之上市前審查程序。第510(k)條途徑適用於與已合法上市器材(predicate device)實質等效之器材,而上市前核准(PMA)則為最高風險等級(Class III)器材所要求。臨床證據可能引用NCT編號之試驗登記,或PMID編號之同行評審文獻。所有產品名稱、公司名稱、識別碼及統一資源定位符(URL)均保留原文,以確保可追溯性及法規提交之完整性。
決定相當於

器材摘要

Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Incorporated. It received FDA 510(k) clearance on 2021-05-24 under 510(k) number K210975. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia?

Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia is a medical device that received FDA 510(k) clearance on 2021-05-24. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K210975.

When did Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia receive FDA 510(k) clearance?

Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia received FDA 510(k) clearance on 2021-05-24, under 510(k) number K210975.

Who is the listed applicant for Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia?

The FDA 510(k) record lists Bausch & Lomb, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia?

The FDA product code for Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia is LPL.

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其他以 Bausch & Lomb, Incorporated 為申請人之記錄

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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

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