FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VFS1 Bipolar Electrosurgical Generator

K Number: K200169 · Decision May 14, 2020
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
112

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Basic Information

Device Name
VFS1 Bipolar Electrosurgical Generator
K Number
K200169
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
FHC, Inc.
Date Received
January 23, 2020
Decision Date
May 14, 2020
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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