FDA 510(k) Application Details - K110370

Device Classification Name	More FDA Info for this Device
510(K) Number	K110370
Device Name	Q-CLEAR
Applicant	LIGHT AGE, INC. 500 APGAR DRIVE SOMERSET, NJ 08873-1150 US Other 510(k) Applications for this Company
Contact	ELIZABETH REDDINGTON Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PDZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2011
Decision Date	09/15/2011
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