Sphincterotome
K-Number: K222421 · 2023-05-03
Device Summary
Frequently Asked Questions
What is the Sphincterotome?
Sphincterotome is a medical device that received FDA 510(k) clearance on 2023-05-03. The listed applicant is Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K222421.
When did Sphincterotome receive FDA 510(k) clearance?
Sphincterotome received FDA 510(k) clearance on 2023-05-03, under 510(k) number K222421.
Who is the listed applicant for Sphincterotome?
The FDA 510(k) record lists Hangzhou AGS MedTech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sphincterotome?
The FDA product code for Sphincterotome is KNS.
Other records listing Hangzhou AGS MedTech Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KNS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.