Single Use Hemoclip
K-Number: K172762 · 2018-03-20
Decision Date2018-03-20
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Single Use Hemoclip is a medical device manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-03-20 under approval number K172762. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Single Use Hemoclip?
Single Use Hemoclip is a medical device that received FDA 510(k) clearance on 2018-03-20. It is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K172762.
When was Single Use Hemoclip approved by the FDA?
Single Use Hemoclip received FDA 510(k) clearance on 2018-03-20, under approval number K172762.
What company makes Single Use Hemoclip?
Single Use Hemoclip is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd..
What is the FDA product code for Single Use Hemoclip?
The FDA product code for Single Use Hemoclip is PKL.
Other Devices by Zhejiang Chuangxiang Medical Technology Co., Ltd.
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K182556SureClip Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd.
K180325Single Use MultiClip DeviceMicro-Tech (Nanjing) Co., Ltd.
K172727HemoclipHangzhou AGS MedTech Co., Ltd.
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.