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FDA 510(k)

Polypectomy Snare

K-Number: K172729 · 2018-05-21

Decision Date2018-05-21
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 2018-05-21 under approval number K172729. 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 2018-05-21. It is manufactured by Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K172729.

When was Polypectomy Snare approved by the FDA?

Polypectomy Snare received FDA 510(k) clearance on 2018-05-21, under approval number K172729.

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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Related Devices (Code: FDI)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.