FDA 510(k) Application Details - K072035

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K072035
Device Name	Light, Ultraviolet, Dermatological
Applicant	ALLUX MEDICAL 1430 O'BRIEN DRIVE SUITE F MENLO PARK, CA 94025 US Other 510(k) Applications for this Company
Contact	LLOYD H GRIESE Other 510(k) Applications for this Contact
Regulation Number	878.4630   More FDA Info for this Regulation Number
Classification Product Code	FTC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/25/2007
Decision Date	10/16/2007
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