Alleye
K 號：K180895 · 2018-06-27
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決定日期2018-06-27
產品代碼HOQ
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
Alleye is the device name listed in this FDA 510(k) record. The listed applicant is Oculocare Medical AG. It received FDA 510(k) clearance on 2018-06-27 under 510(k) number K180895. The device is classified under product code HOQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Alleye?
Alleye is a medical device that received FDA 510(k) clearance on 2018-06-27. The listed applicant is Oculocare Medical AG. The 510(k) number is K180895.
When did Alleye receive FDA 510(k) clearance?
Alleye received FDA 510(k) clearance on 2018-06-27, under 510(k) number K180895.
Who is the listed applicant for Alleye?
The FDA 510(k) record lists Oculocare Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alleye?
The FDA product code for Alleye is HOQ.
相關臨床試驗
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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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