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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name powered laser surgical instrument
510(k) Number K232117
Device Name Diode Laser Hair Removal (LHR-V6S-1064, LHR-V6S/B-1064)
Applicant
Wuhan Lotuxs Technology Co., Ltd.
501/E2, No.999 High-tech Avenue
Wuhan,  CN 430206
Applicant Contact Na Wu
Correspondent
Wuhan Lotuxs Technology Co., Ltd.
501/E2, No.999 High-tech Avenue
Wuhan,  CN 430206
Correspondent Contact Na Wu
Regulation Number878.4810
Classification Product Code
GEX  
Subsequent Product Code
OHT  
Date Received07/17/2023
Decision Date 11/28/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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