FDA 510(k) Application Details - K251042

Device Classification Name Light Based Over The Counter Wrinkle Reduction

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510(K) Number K251042
Device Name Light Based Over The Counter Wrinkle Reduction
Applicant Guangzhou Ahead Intelligent Technology Co., Ltd.
Room 505, Building 2, No.10, Industrial 1st Road,
Zhicun, Pashi Street, Panyu
Guangzhou 511430 CN
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Contact Zheng Leo
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Regulation Number 878.4810

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Classification Product Code OHS
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Date Received 04/03/2025
Decision Date 06/06/2025
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 K251042


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