Single Use Grasping Forceps— 510(k) K191900

Name: FDA 510(k) clearance K191900
Creator: U.S. Food and Drug Administration
Published: 2020-03-27

Substantially Equivalent

Zhejiang Chuangxiang Medical Technology Co., Ltd.

FDA 510(k) clearance K191900 for Single Use Grasping Forceps, Substantially Equivalent on 2020-03-27. Applicant: Zhejiang Chuangxiang Medical Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Zhejiang Chuangxiang Medical Technology Co., Ltd.
Product code: Code OCZ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2019-07-16
Decision date: 2020-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hanzhou, CN

Download summary PDF View on FDA.gov ↗

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