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FDA 510(k) Application Details - K241203
Device Classification Name
Light Based Over The Counter Wrinkle Reduction
More FDA Info for this Device
510(K) Number
K241203
Device Name
Light Based Over The Counter Wrinkle Reduction
Applicant
Dongguan Hunter Electronic Technology Co., Ltd.
Room 301, Building 6, 74 Qiaodong Road, Tangxia Town
Guangdong 523728 CN
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Contact
Hunter Ye
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
OHS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/30/2024
Decision Date
07/25/2024
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
FDA Source Information for K241203
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