FDA 510(k) Application Details - K042502

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K042502
Device Name	Light, Ultraviolet, Dermatological
Applicant	DAAVLIN DISTRIBUTING CO. 205 WEST BEMENT ST. BRYAN, OH 43506 US Other 510(k) Applications for this Company
Contact	DAVID W SWANSON 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	09/14/2004
Decision Date	10/14/2004
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