FDA 510(k) Application Details - K021092

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K021092
Device Name	Light, Ultraviolet, Dermatological
Applicant	PHILIPS LIGHTING CO. 200 FRANKLIN SQ. DR. P.O. BOX 6800 SOMERSET, NJ 08875-6800 US Other 510(k) Applications for this Company
Contact	TONI J HOFFMANN 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	04/04/2002
Decision Date	05/16/2002
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