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

Dr.MUSIC 3s

K Number: K172451 · Decision Nov 17, 2017
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
1
Review Days
95

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Basic Information

Device Name
Dr.MUSIC 3s
K Number
K172451
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smartmedicaldevice Co., Ltd.
Date Received
August 14, 2017
Decision Date
November 17, 2017
Product Code
NUH
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

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