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)

一次性尼龍檢查手套(已測試與化療藥物使用)

K 號:K212919 · 2021-12-15

決定日期2021-12-15
產品代碼LZA
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

Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is the device name listed in this FDA 510(k) record. The listed applicant is Jiujiang Taixin Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-12-15 under 510(k) number K212919. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is a medical device that received FDA 510(k) clearance on 2021-12-15. The listed applicant is Jiujiang Taixin Technology Co., Ltd.. The 510(k) number is K212919.

When did Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) receive FDA 510(k) clearance?

Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) received FDA 510(k) clearance on 2021-12-15, under 510(k) number K212919.

Who is the listed applicant for Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

The FDA 510(k) record lists Jiujiang Taixin Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)?

The FDA product code for Disposable Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs) is LZA.

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 Jiujiang Taixin Technology Co., Ltd. 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:LZA)

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。

↑