FDA 510(k) Application Details - K033448

Device Classification Name	Purifier, Air, Ultraviolet, Medical   More FDA Info for this Device
510(K) Number	K033448
Device Name	Purifier, Air, Ultraviolet, Medical
Applicant	JOHN MFG., LTD. 18780 AMAR ROAD, STE 203-203 WALNUT, CA 91789 US Other 510(k) Applications for this Company
Contact	ARTHUR KING MA 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	10/29/2003
Decision Date	07/12/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review