FDA 510(k) Application Details - K031800

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K031800
Device Name	Light, Ultraviolet, Dermatological
Applicant	SOLARC SYSTEMS, INC. 12 PARKER COURT BARRIE, ONTARIO L4N 2A6 CA Other 510(k) Applications for this Company
Contact	BRUCE ELLIOTT 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	06/11/2003
Decision Date	09/10/2003
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