Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


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 BK220687
Tradename LIPISYSTEMS AQUAVAGE MODELS AV2000 AND AV1200 (K092284)
Device Name Lipoaspirate washing system for aesthetic body contouring
Original Applicant
Medical Device Resource Corp
23392 connecticut st
hayward,  CA  94545
Regulation Number878.5040
Classification Product Code
QKL  
Date Received03/28/2022
Decision Date 09/01/2009
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
Type 510(k) Special
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product No
-
-