FDA 510(k) Application Details - K001767

Device Classification Name	Antigen, Iha, Cytomegalovirus   More FDA Info for this Device
510(K) Number	K001767
Device Name	Antigen, Iha, Cytomegalovirus
Applicant	DIAMEDIX CORP. 2140 NORTH MIAMI AVE. MIAMI, FL 33127 US Other 510(k) Applications for this Company
Contact	LYNNE STIRLING Other 510(k) Applications for this Contact
Regulation Number	866.3175   More FDA Info for this Regulation Number
Classification Product Code	LJO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/12/2000
Decision Date	08/07/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review