FDA 510(k) Application Details - K041212

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K041212
Device Name	Light, Ultraviolet, Dermatological
Applicant	NATIONAL BIOLOGICAL CORP. 1532 ENTERPRISE PKWY. TWINSBURG, OH 44087 US Other 510(k) Applications for this Company
Contact	LORETTA MOONEY 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	05/10/2004
Decision Date	06/09/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review