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

Single Use Irrigation bipolar cable

K Number: K211170 · Decision Oct 19, 2021
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
4
Review Days
183

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Basic Information

Device Name
Single Use Irrigation bipolar cable
K Number
K211170
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Modern Medical Equipment Manufacturing, Ltd.
Date Received
April 19, 2021
Decision Date
October 19, 2021
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K Number Device Name
K210315 Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar Forceps with Smoke Evacuation, Single Use Hand Switch Monopolar Forceps, Single Use Hand Switch Bipolar Forceps
K200372 Smoke Evacuation Fingerswitch, Smoke evacuation system with electrosurgical pencil
K192542 Foot Control Electrosurgical Pencil, Push Button Electrosurgical Pencil, Rocker Switch Electrosurgical Pencil, Holster, Electorde