Bipolar Coagulation Foreceps
K-Number: K210406 · 2021-10-05
Device Summary
Frequently Asked Questions
What is the Bipolar Coagulation Foreceps?
Bipolar Coagulation Foreceps is a medical device that received FDA 510(k) clearance on 2021-10-05. The listed applicant is Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K210406.
When did Bipolar Coagulation Foreceps receive FDA 510(k) clearance?
Bipolar Coagulation Foreceps received FDA 510(k) clearance on 2021-10-05, under 510(k) number K210406.
Who is the listed applicant for Bipolar Coagulation Foreceps?
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 Bipolar Coagulation Foreceps?
The FDA product code for Bipolar Coagulation Foreceps is KGE.
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: KGE)
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.