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FDA 510(k)

Sphincterotome

K-Number: K222421 · 2023-05-03

Decision Date2023-05-03
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Sphincterotome is a medical device manufactured by Hangzhou AGS MedTech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-03 under approval number K222421. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sphincterotome?

Sphincterotome is a medical device that received FDA 510(k) clearance on 2023-05-03. It is manufactured by Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K222421.

When was Sphincterotome approved by the FDA?

Sphincterotome received FDA 510(k) clearance on 2023-05-03, under approval number K222421.

What company makes Sphincterotome?

Sphincterotome is manufactured by Hangzhou AGS MedTech Co., Ltd..

What is the FDA product code for Sphincterotome?

The FDA product code for Sphincterotome is KNS.

Other Devices by Hangzhou AGS MedTech Co., Ltd.

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Related Devices (Code: KNS)

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.