FDA 510(k) Application Details - K243957

Device Classification Name Powered Laser Surgical Instrument

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510(K) Number K243957
Device Name Powered Laser Surgical Instrument
Applicant WONTECH CO., LTD.
64 Techno 8-ro, Yuseong-gu
Daejeon 34028 KR
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Contact Hyunsik Yoon
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Regulation Number 878.4810

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Classification Product Code GEX
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Date Received 12/23/2024
Decision Date 03/12/2025
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 K243957


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