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

Electrosurgical System (Electrosurgical Generator with Bipolar polypectomy snare combination and Single use electrosurgical knife combination accessories)

K Number: K192342 · Decision May 21, 2020
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
17
Review Days
267

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Electrosurgical System (Electrosurgical Generator with Bipolar polypectomy snare combination and Single use electrosurgical knife combination accessories)
K Number
K192342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hangzhou AGS MedTech Co., Ltd.
Date Received
August 28, 2019
Decision Date
May 21, 2020
Product Code
KNS
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
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNS), ordered by most recent decision date.

View all

Other Clearances by Hangzhou AGS MedTech Co., Ltd.

K Number Device Name
K252270 Hemoclip
K252271 Hemoclip
K241704 Endoscopic Water Pump
K222421 Sphincterotome
K221713 Polypectomy Snare
K213143 Hemoclip
K213578 Balloon Dilatation Catheter
K211787 Hemoclip
K210406 Bipolar Coagulation Foreceps
K201121 Sphincterotome
Search all 17 clearances from Hangzhou AGS MedTech Co., Ltd. →