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

Electrode Handpieces (VCT, RFTV, BMDT series)

K Number: K232763 · Decision Oct 4, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
4
Review Days
26

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Basic Information

Device Name
Electrode Handpieces (VCT, RFTV, BMDT series)
K Number
K232763
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
RF Medical Co., Ltd.
Date Received
September 8, 2023
Decision Date
October 4, 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

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