FDA 510(k) Application Details - K130152

Device Classification Name	System, Suction, Lipoplasty   More FDA Info for this Device
510(K) Number	K130152
Device Name	System, Suction, Lipoplasty
Applicant	ANDREW TECHNOLOGIES, LLC 3 Haddon Avenue Haddonfield, NJ 08033 US Other 510(k) Applications for this Company
Contact	HERBERT CRANE 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	01/22/2013
Decision Date	04/18/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review