Polypectomy Snare
K-Number: K221713 · 2023-03-03
ApplicantHangzhou AGS MedTech Co., Ltd.
Decision Date2023-03-03
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Polypectomy Snare is a medical device manufactured by Hangzhou AGS MedTech Co., Ltd.. It received FDA 510(k) clearance on 2023-03-03 under approval number K221713. 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 Polypectomy Snare?
Polypectomy Snare is a medical device that received FDA 510(k) clearance on 2023-03-03. It is manufactured by Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K221713.
When was Polypectomy Snare approved by the FDA?
Polypectomy Snare received FDA 510(k) clearance on 2023-03-03, under approval number K221713.
What company makes Polypectomy Snare?
Polypectomy Snare is manufactured by Hangzhou AGS MedTech Co., Ltd..
What is the FDA product code for Polypectomy Snare?
The FDA product code for Polypectomy Snare is FDI.
Other Devices by Hangzhou AGS MedTech 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.