FDA 510(k)

Clariti 1日多焦距（somofilcon A）柔軟（親水），每日抛弃式帶防紫外線鏡片

K 號：K234127 · 2024-01-25

決定日期2024-01-25

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

Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 2024-01-25 under 510(k) number K234127. 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 Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker?

Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker is a medical device that received FDA 510(k) clearance on 2024-01-25. The listed applicant is CooperVision, Inc.. The 510(k) number is K234127.

When did Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker receive FDA 510(k) clearance?

Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker received FDA 510(k) clearance on 2024-01-25, under 510(k) number K234127.

Who is the listed applicant for Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker?

The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker?

The FDA product code for Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker is LPL.

其他以 CooperVision, Inc. 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。

K220070MyDay（stenfilcon A）柔軟（親水）每日抛弃式隱形眼鏡，Avaira Vitality（fanfilcon A）柔軟（親水）隱形眼鏡 K213164Avaira Vitality K202756Clariti 1 天 (somofilcon A)，Clariti 1 天適應散光 (somofilcon A)，Clariti 1 天多焦距 (somofilcon A)，Clariti 1 天多焦距適應散光 (somofilcon A)K191763MyDay (Stenfilcon A) ASPHERE、MyDay (Stenfilcon A) TORIC、MyDay (Stenfilcon A) 多焦距、MyDay (Stenfilcon A) 多焦距TORIC K190965MyDay K181920Clariti 1日（somofilcon A）柔軟（親水）每日抛弃式隱形眼鏡鏡片，具有防紫外線功能

查看所有 8 項裝置 →

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。