FDA 510(k) Application Details - K092284

Device Classification Name	System, Suction, Lipoplasty   More FDA Info for this Device
510(K) Number	K092284
Device Name	System, Suction, Lipoplasty
Applicant	MEDICAL DEVICE RESOURCE CORP. 23392 CONNECTICUT ST. HAYWARD, CA 94545 US Other 510(k) Applications for this Company
Contact	MELBOURNE KIMSEY 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	07/29/2009
Decision Date	09/01/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review