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FDA 510(k)

HALYARD* 紫色丁腈 – XTRA* 非粉塵檢查手套

K 號:K160709 · 2016-09-06

決定日期2016-09-06
產品代碼LZC
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

HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves is the device name listed in this FDA 510(k) record. The listed applicant is Halyard Health. It received FDA 510(k) clearance on 2016-09-06 under 510(k) number K160709. The device is classified under product code LZC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves?

HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves is a medical device that received FDA 510(k) clearance on 2016-09-06. The listed applicant is Halyard Health. The 510(k) number is K160709.

When did HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves receive FDA 510(k) clearance?

HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves received FDA 510(k) clearance on 2016-09-06, under 510(k) number K160709.

Who is the listed applicant for HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves?

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

What is the FDA product code for HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves?

The FDA product code for HALYARD* PURPLE NITRILE – XTRA* Powder-Free Exam Gloves is LZC.

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 Halyard Health 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:LZC)

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

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