FDA 510(k) Application Details - K232424

Device Classification Name

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510(K) Number K232424
Device Name CurrentBody Skin RF
Applicant EL Global Trade Ltd.
6th Ha-Gavish St.
Netanya 4250706 IL
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Contact Sivan Fishman
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Regulation Number

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Classification Product Code PAY
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Date Received 08/11/2023
Decision Date 03/06/2024
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 K232424


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