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

VYBE RF Electrosurgical System

K Number: K230968 · Decision Jul 6, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
92

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
VYBE RF Electrosurgical System
K Number
K230968
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ShenB Co., Ltd.
Date Received
April 5, 2023
Decision Date
July 6, 2023
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.

View all

Other Clearances by ShenB Co., Ltd.

K Number Device Name
K253926 Diacore
K251649 Sunny Plus (Sunny)
K242241 Sunny
K241535 Vybe RF II
K232223 PlaDuo System
K221363 AF Laser
K211562 Virtue RF
K193070 VIVACE Electrosurgical Device
K202415 VirtueRF
K201735 PlaDuo System
Search all 11 clearances from ShenB Co., Ltd. →