FDA 510(k)

單次使用抓取镊子

K 號：K191900 · 2020-03-27

申請人Zhejiang Chuangxiang Medical Technology Co., Ltd.

決定日期2020-03-27

產品代碼OCZ

諮詢委員會GU

決定相當於

器材摘要

Single Use Grasping Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-03-27 under 510(k) number K191900. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Single Use Grasping Forceps?

Single Use Grasping Forceps is a medical device that received FDA 510(k) clearance on 2020-03-27. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K191900.

When did Single Use Grasping Forceps receive FDA 510(k) clearance?

Single Use Grasping Forceps received FDA 510(k) clearance on 2020-03-27, under 510(k) number K191900.

Who is the listed applicant for Single Use Grasping Forceps?

FDA 510(k) 記錄將浙江創想醫療技術有限公司列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for Single Use Grasping Forceps?

The FDA product code for Single Use Grasping Forceps is OCZ.

其他以 Zhejiang Chuangxiang Medical 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。

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相關器械（代碼：OCZ）

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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