FDA 510(k)

德西歐（hioxifilcon D）每日佩戴柔軟（親水）隐形眼鏡（透明及著色）

K 號：K181050 · 2018-06-13

決定日期2018-06-13

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

Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) is the device name listed in this FDA 510(k) record. The listed applicant is Qualimed Srl. It received FDA 510(k) clearance on 2018-06-13 under 510(k) number K181050. 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 Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted)?

Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) is a medical device that received FDA 510(k) clearance on 2018-06-13. The listed applicant is Qualimed Srl. The 510(k) number is K181050.

When did Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) receive FDA 510(k) clearance?

Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) received FDA 510(k) clearance on 2018-06-13, under 510(k) number K181050.

Who is the listed applicant for Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted)?

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

What is the FDA product code for Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted)?

The FDA product code for Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) is LPL.

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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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：LPL）

官方來源