FDA 510(k)

Vitreq一次性激光探針、光纖和燈籠

K 號：K182646 · 2019-05-01

決定日期2019-05-01

產品代碼HQB

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

Vitreq disposable laser probes, light fibers and Chandelier is the device name listed in this FDA 510(k) record. The listed applicant is VitreQ BV. It received FDA 510(k) clearance on 2019-05-01 under 510(k) number K182646. The device is classified under product code HQB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vitreq disposable laser probes, light fibers and Chandelier?

Vitreq disposable laser probes, light fibers and Chandelier is a medical device that received FDA 510(k) clearance on 2019-05-01. The listed applicant is VitreQ BV. The 510(k) number is K182646.

When did Vitreq disposable laser probes, light fibers and Chandelier receive FDA 510(k) clearance?

Vitreq disposable laser probes, light fibers and Chandelier received FDA 510(k) clearance on 2019-05-01, under 510(k) number K182646.

Who is the listed applicant for Vitreq disposable laser probes, light fibers and Chandelier?

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

What is the FDA product code for Vitreq disposable laser probes, light fibers and Chandelier?

The FDA product code for Vitreq disposable laser probes, light fibers and Chandelier is HQB.

其他以 VitreQ BV 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。

K202038冷凍治療設備

相關器械（代碼：HQB）

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。

K220263迴流外科雷射探針，迴流外科照明雷射探針，迴流外科內視鏡照明器，迴流外科灯具Vortex Surgical, Inc.K191846MAXReach 激光探針Vortex Surgical, Inc.

官方來源

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