FDA 510(k) Application Details - K250413

Device Classification Name Light Based Over The Counter Wrinkle Reduction

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510(K) Number K250413
Device Name Light Based Over The Counter Wrinkle Reduction
Applicant Shenzhen Perfect Idea Technology Limited
4F, Building 1, Fuhua Industrial Park, Tangwei,
Fuyong, BaoÆan
Shenzhen 518103 CN
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Contact Zhuo Zhan
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Regulation Number 878.4810

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Classification Product Code OHS
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Date Received 02/13/2025
Decision Date 03/18/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K250413


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