FDA 510(k) Application Details - K023830

Device Classification Name	Purifier, Air, Ultraviolet, Medical   More FDA Info for this Device
510(K) Number	K023830
Device Name	Purifier, Air, Ultraviolet, Medical
Applicant	KES SCIENCE & TECHNOLOGY, INC 3625 KENNESAW N.INDUSTRIAL PKY KENNESAW, GA 30144 US Other 510(k) Applications for this Company
Contact	JOHN HAYMAN, JR Other 510(k) Applications for this Contact
Regulation Number	880.6500   More FDA Info for this Regulation Number
Classification Product Code	FRA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/18/2002
Decision Date	02/04/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review