FDA 510(k) Application Details - K121703

Device Classification Name	System, Suction, Lipoplasty   More FDA Info for this Device
510(K) Number	K121703
Device Name	System, Suction, Lipoplasty
Applicant	MEDI-KHAN USA, INC 399 MASSACHUSETTS AVE. #2 BOSTON, MA 02115 US Other 510(k) Applications for this Company
Contact	KACHI ENYINNA Other 510(k) Applications for this Contact
Regulation Number	878.5040   More FDA Info for this Regulation Number
Classification Product Code	MUU Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/08/2012
Decision Date	12/07/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review