FDA 510(k) Application Details - K993085

Device Classification Name	System, Test, Anticardiolipin Immunological   More FDA Info for this Device
510(K) Number	K993085
Device Name	System, Test, Anticardiolipin Immunological
Applicant	COGENT DIAGNOTICS LTD. 7272 CHAPMAN AVE. GARDEN GROVE, CA 92841 US Other 510(k) Applications for this Company
Contact	RANDY WILSON Other 510(k) Applications for this Contact
Regulation Number	866.5660   More FDA Info for this Regulation Number
Classification Product Code	MID Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/15/1999
Decision Date	02/01/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review