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

Secret RF Smartcure Applicator with electrodes

K Number: K182355 · Decision Sep 6, 2019
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
372

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Basic Information

Device Name
Secret RF Smartcure Applicator with electrodes
K Number
K182355
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
Ilooda Co,., Ltd.
Date Received
August 30, 2018
Decision Date
September 6, 2019
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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K212561 MTX-C1
K222555 reepot Nd; YAG laser system
K213250 Secret Duo
K211000 ACUTRON
K202043 Secret Duo
K173474 RetiCapture
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