FDA 510(k)

丁腈檢查手套無菌且經測試可用於化療藥物之宣稱，白色

K 號：K190725 · 2019-12-17

決定日期2019-12-17

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

Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White is the device name listed in this FDA 510(k) record. The listed applicant is Riverstone Resources Sdn Bhd. It received FDA 510(k) clearance on 2019-12-17 under 510(k) number K190725. 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 Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White?

Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White is a medical device that received FDA 510(k) clearance on 2019-12-17. The listed applicant is Riverstone Resources Sdn Bhd. The 510(k) number is K190725.

When did Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White receive FDA 510(k) clearance?

Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White received FDA 510(k) clearance on 2019-12-17, under 510(k) number K190725.

Who is the listed applicant for Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White?

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

What is the FDA product code for Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White?

The FDA product code for Nitrile Examination Glove Sterile Tested for use with Chemotherapy Drugs Claim, White is LZA.

其他以 Riverstone Resources 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。

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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。

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官方來源

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