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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name electrosurgical, cutting & coagulation & accessories
510(k) Number K193355
Device Name Electrodes Handpieces for Mygen V-1000 RF System
Applicant
RF Medical Co., Ltd
#502, 503, 506, 511, 254, Beotkkot-ro, Geumcheon-gu
seoul,  KR
Applicant Contact kwang s choi
Correspondent
MTech Group
7707 Fannin St. Ste 200 V111
houston,  TX  77054
Correspondent Contact dave kim
Regulation Number878.4400
Classification Product Code
GEI  
Date Received12/04/2019
Decision Date 08/03/2020
Decision substantially equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
summary summary
Type Special
Reviewed by Third Party No
Combination Product No
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