FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

VIVA combo RF System

K Number: K252833 · Decision May 26, 2026
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
263

Basic Information

Device Name
VIVA combo RF System
K Number
K252833
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
Starmed Co., Ltd.
Date Received
September 5, 2025
Decision Date
May 26, 2026
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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K203795 Star RF Electrode, VIVA RF Electrode
K181758 ELRA Electrode
K183538 VIVA combo RF System
K181249 EUSRA RF Electrode
K172012 star RF Electrode, VIVA RF Electrode
K163450 VIVA combo RF System
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