FDA 510(k) Application Details - K063235

Device Classification Name	More FDA Info for this Device
510(K) Number	K063235
Device Name	CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT
Applicant	CYTORI THERAPEUTICS, INC. 3020 CALLAN ROAD SAN DIEGO, CA 92121-1109 US Other 510(k) Applications for this Company
Contact	KENNETH K KLEINHENZ 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	10/25/2006
Decision Date	01/24/2007
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