FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Ulike Clear Zero (YC10 BU)

K Number: K260895 · Decision May 28, 2026
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
77
Applicant Total
1
Review Days
71

Basic Information

Device Name
Ulike Clear Zero (YC10 BU)
K Number
K260895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guangxi Ulike Medical Technology Co., Ltd.
Date Received
March 18, 2026
Decision Date
May 28, 2026
Product Code
NFO
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
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

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