免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

Renasys-F XL 泡沫敷料組搭配柔軟端口,Renasys XL 透明膠膜敷料

K 號:K202783 · 2022-01-14

決定日期2022-01-14
產品代碼OMP
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Medical Limited. It received FDA 510(k) clearance on 2022-01-14 under 510(k) number K202783. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing?

Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing is a medical device that received FDA 510(k) clearance on 2022-01-14. The listed applicant is Smith & Nephew Medical Limited. The 510(k) number is K202783.

When did Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing receive FDA 510(k) clearance?

Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing received FDA 510(k) clearance on 2022-01-14, under 510(k) number K202783.

Who is the listed applicant for Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing?

The FDA 510(k) record lists Smith & Nephew Medical Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing?

The FDA product code for Renasys-F XL Foam Dressing Kit With Soft Port, Renasys XL Transparent Film Dressing is OMP.

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。

其他以 Smith & Nephew Medical Limited 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。

查看所有 21 項裝置 →

相關器械(代碼:OMP)

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。

↑