FDA 510(k) Application Details - K063621

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K063621
Device Name	Light, Ultraviolet, Dermatological
Applicant	DAAVLIN CO. 205 WEST BEMENT ST. P.O. BOX 626 BRYAN, OH 43506 US Other 510(k) Applications for this Company
Contact	TARA MANSUR 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	12/05/2006
Decision Date	01/17/2007
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