FDA 510(k) Application Details - K081039

Device Classification Name	More FDA Info for this Device
510(K) Number	K081039
Device Name	LIPO CANNULA
Applicant	MILLENNIUM MEDICAL TECHNOLOGIES, INC. 7055 DIVOT DR. LAVERNE, CA 91750 US Other 510(k) Applications for this Company
Contact	GREGORY M MILES 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	04/11/2008
Decision Date	07/10/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review