FDA 510(k) Application Details - K052183

Device Classification Name	More FDA Info for this Device
510(K) Number	K052183
Device Name	SORING GMBH SONOCA LIPO
Applicant	SORING GMBH MEDIZINTECHNIK 1600 MANCHESTER WAY CORINTH, TX 76210 US Other 510(k) Applications for this Company
Contact	CARL ALLETTO Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QPB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/10/2005
Decision Date	10/07/2005
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