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U.S. Department of Health and Human Services

510(k) Premarket Notification
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New Search Biologics Clearance Letters and 510(k) Summaries Back To Search Results
Device Classification Name lipoaspirate washing system for aesthetic body contouring
510(k) Number BK220717
Tradename AuraGen 123 Suction Lipoplasty System (A123) (K190278)
Device Name Lipoaspirate washing system for aesthetic body contouring
Regulation Number878.5040
Classification Product Code
QKL  
Date Received04/05/2022
Decision Date 05/03/2019
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
Type 510(k) Traditional
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product No
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