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

Smoklean

K Number: K173108 · Decision May 18, 2018
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
9
Review Days
231

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Basic Information

Device Name
Smoklean
K Number
K173108
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sejong Medical Co., Ltd.
Date Received
September 29, 2017
Decision Date
May 18, 2018
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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K Number Device Name
K253165 LAP-iX2N
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K200638 LAP-iX Suction Irrigation
K173111 LAP-iX Suction Irrigation
K173112 LAP-iX
K171726 LapBag
K171741 Laport