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)

非无菌無粉乳膠檢查手套

K 號:K221667 · 2022-10-28

決定日期2022-10-28
產品代碼LYY
諮詢委員會醫療設備規範文本翻譯如下: HO 注意:原文中未提供具體的醫療設備規範文本,因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於

器材摘要

Non Sterile Powder Free Latex Examination Glove is the device name listed in this FDA 510(k) record. The listed applicant is New Era Medicare Sdn. Bhd.. It received FDA 510(k) clearance on 2022-10-28 under 510(k) number K221667. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Non Sterile Powder Free Latex Examination Glove?

Non Sterile Powder Free Latex Examination Glove is a medical device that received FDA 510(k) clearance on 2022-10-28. The listed applicant is New Era Medicare Sdn. Bhd.. The 510(k) number is K221667.

When did Non Sterile Powder Free Latex Examination Glove receive FDA 510(k) clearance?

Non Sterile Powder Free Latex Examination Glove received FDA 510(k) clearance on 2022-10-28, under 510(k) number K221667.

Who is the listed applicant for Non Sterile Powder Free Latex Examination Glove?

The FDA 510(k) record lists New Era Medicare Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Non Sterile Powder Free Latex Examination Glove?

The FDA product code for Non Sterile Powder Free Latex Examination Glove is LYY.

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 New Era Medicare Sdn. Bhd. 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。

相關器械(代碼:LYY)

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。

↑