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FDA 510(k)

Clalen 54（hioxifilcon D）柔軟（親水）日戴隐形眼鏡，Clalen 58（hioxifilcon A）柔軟（親水）日戴隐形眼鏡

K 號：K153766 · 2016-04-08

申請人INTEROJO, Inc.
決定日期2016-04-08
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

Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear is the device name listed in this FDA 510(k) record. The listed applicant is INTEROJO, Inc.. It received FDA 510(k) clearance on 2016-04-08 under 510(k) number K153766. 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 Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear?

Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear is a medical device that received FDA 510(k) clearance on 2016-04-08. The listed applicant is INTEROJO, Inc.. The 510(k) number is K153766.

When did Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear receive FDA 510(k) clearance?

Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear received FDA 510(k) clearance on 2016-04-08, under 510(k) number K153766.

Who is the listed applicant for Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear?

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

What is the FDA product code for Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear?

The FDA product code for Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) Soft (hydrophilic) Contact Lens for Daily Wear is LPL.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 INTEROJO, 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。

K260507Interojo 45（inofilcon A）柔軟（親水）矽膠水凝片鏡，搭配GrabSoo PlusK221517POLYVUE（聚麥康）柔軟（親水）隱形眼鏡，POLYVUE COLOR（聚麥康）柔軟（親水）隱形眼鏡

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。

K262495美如1日上昇（米法立酮A）Menicon Co, Ltd.K260507Interojo 45（inofilcon A）柔軟（親水）矽膠水凝片鏡，搭配GrabSoo PlusINTEROJO, Inc.K253352Pegavision (Polymacon) 每日抛弃式柔軟（親水）隱形眼鏡；Pegavision (Polymacon) 柔軟（親水）隱形眼鏡；Pegavision (Polymacon) 彩色每日抛弃式柔軟（親水）隱形眼鏡；Pegavision (Polymacon) 彩色柔軟（親水）隱形眼鏡Pegavision CorporationK261299Pegavision (Toufilcon B) 每日抛弃式柔軟（親水）隱形眼鏡；Pegavision (Toufilcon B) 柔軟（親水）隱形眼鏡Pegavision CorporationK253885PUSCON 水平衡-1日顏色調節 (omafilcon A) 轟軟 (親水) 接觸鏡片；PUSCON 水平衡-1日顏色 (omafilcon A) 轟軟 (親水) 接觸鏡片GEO MEDICAL CO., LTD.K254269Saview SH Optic 38 UV (Senofilcon A) 可見度著色軟性（親水）隱形眼鏡；Saview SH Optic 38 UV 球面（Senofilcon A）可見度著色軟性（親水）隱形眼鏡；Saview SH Optic 38 UV 多焦距（Senofilcon A）可見度著色軟性（親水）隱形眼鏡St. shine Optical Co., Ltd.

官方來源

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