FDA 510(k) Application Details - K031881

Device Classification Name	More FDA Info for this Device
510(K) Number	K031881
Device Name	AIRBRUSH LIPOSCULPTOR SYSTEM
Applicant	BIOSCULPTURE TECHNOLOGY, INC. 120 CENTRAL PARK SOUTH NEW YORK, NY 10019 US Other 510(k) Applications for this Company
Contact	ROBERT CUCIN 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	06/18/2003
Decision Date	07/28/2003
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	Y
Expedited Review