FDA 510(k) Application Details - K010311

Device Classification Name	More FDA Info for this Device
510(K) Number	K010311
Device Name	LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE
Applicant	EUROMI SA P.O. BOX 2156 HUNTINGTON, CT 06484 US Other 510(k) Applications for this Company
Contact	JOSEPH M AZARY 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	02/01/2001
Decision Date	06/29/2001
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