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

VIVA combo RF System

K Number: K163450 · Decision Mar 8, 2017
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
90

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Basic Information

Device Name
VIVA combo RF System
K Number
K163450
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
December 8, 2016
Decision Date
March 8, 2017
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

Similar 510(k) Clearances

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

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Other Clearances by Starmed Co., Ltd.

K Number Device Name
K252833 VIVA combo RF System
K251566 TS-RF Generator (STS10)
K234140 VIVA combo RF System (VIVA combo RF System)
K222997 VVR Generator system
K233113 ELRA Electrode (7-2B11S, 7-2B11L, 7-2B22S, 7-2B22L, 7-4B18S, 7-4B18L, 7-4B33S, 7-4B33L)
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
Search all 11 clearances from Starmed Co., Ltd. →