FDA 510(k) Application Details - K092482

Device Classification Name	System, Suction, Lipoplasty   More FDA Info for this Device
510(K) Number	K092482
Device Name	System, Suction, Lipoplasty
Applicant	SHIPPERT MEDICAL TECHNOLOGIES CORP. 6248 SOUTH TROY CIRCLE UNIT A CENTENNIAL, CO 80111 US Other 510(k) Applications for this Company
Contact	SARAH L SHIPPERT 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	08/13/2009
Decision Date	12/04/2009
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