• 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) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name system, suction, lipoplasty
510(k) Number K121005
Device Name ADIPREP ADIPOSE TRANSFER SYSTEM
Original Applicant
HARVEST TECHNOLOGIES, CORP.
40 grissom rd, suite 100
plymouth,  MA  02360
Original Contact gabriel j muraca, jr.
Regulation Number878.5040
Classification Product Code
MUU  
Date Received04/03/2012
Decision Date 09/21/2012
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
-
-