FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Hemoclip

K Number: K252270 · Decision Apr 8, 2026
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
62
Applicant Total
17
Review Days
261

Basic Information

Device Name
Hemoclip
K Number
K252270
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4400
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hangzhou AGS MedTech Co., Ltd.
Date Received
July 21, 2025
Decision Date
April 8, 2026
Product Code
PKL
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PKL Hemostatic Metal Clip For The Gi Tract

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K Number Device Name
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K211787 Hemoclip
K210406 Bipolar Coagulation Foreceps
K201121 Sphincterotome
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