FDA 510(k) Application Details - DEN110004

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN110004
Device Name	CABOCHON SYSTEM
Applicant	CABOCHON AESTHETICS, INC. 127 Independence Drive Menlo Park, CA 94025 US Other 510(k) Applications for this Company
Contact	BEN BRIAN Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OUP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/31/2011
Decision Date	07/12/2013
Decision	DENG -
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review