Single Use Grasping Forceps
K-Number: K191900 · 2020-03-27
Decision Date2020-03-27
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Single Use Grasping Forceps is a medical device manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-03-27 under approval number K191900. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
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. It is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K191900.
When was Single Use Grasping Forceps approved by the FDA?
Single Use Grasping Forceps received FDA 510(k) clearance on 2020-03-27, under approval number K191900.
What company makes Single Use Grasping Forceps?
Single Use Grasping Forceps is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd..
What is the FDA product code for Single Use Grasping Forceps?
The FDA product code for Single Use Grasping Forceps is OCZ.
Other Devices by Zhejiang Chuangxiang Medical Technology Co., Ltd.
Related Devices (Code: OCZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.