FDA 510(k) Application Details - K053451

Device Classification Name	More FDA Info for this Device
510(K) Number	K053451
Device Name	LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);
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	12/12/2005
Decision Date	08/25/2006
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