FDA 510(k) Application Details - K072793

Device Classification Name	More FDA Info for this Device
510(K) Number	K072793
Device Name	LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688
Applicant	MOELLER MEDICAL GMBH & CO. KG 23832 VIA MONTE COTO DE CAZA, CA 92679-4001 US Other 510(k) Applications for this Company
Contact	BILL KELLEY 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	10/01/2007
Decision Date	03/04/2008
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