Disposable Polypectomy Snare
K-Number: K213222 · 2022-06-06
ApplicantBeijing Zksk Technology Co., Ltd.
Decision Date2022-06-06
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Disposable Polypectomy Snare is a medical device manufactured by Beijing Zksk Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-06 under approval number K213222. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Disposable Polypectomy Snare?
Disposable Polypectomy Snare is a medical device that received FDA 510(k) clearance on 2022-06-06. It is manufactured by Beijing Zksk Technology Co., Ltd.. The 510(k) number is K213222.
When was Disposable Polypectomy Snare approved by the FDA?
Disposable Polypectomy Snare received FDA 510(k) clearance on 2022-06-06, under approval number K213222.
What company makes Disposable Polypectomy Snare?
Disposable Polypectomy Snare is manufactured by Beijing Zksk Technology Co., Ltd..
What is the FDA product code for Disposable Polypectomy Snare?
The FDA product code for Disposable Polypectomy Snare is FDI.
Other Devices by Beijing Zksk Technology Co., Ltd.
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K173673AcuSnare Polypectomy SnareWilson-Cook Medical, Inc.
K172729Polypectomy SnareHangzhou AGS MedTech Co., Ltd.
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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.