FDA 510(k) Application Details - K013018

Device Classification Name	System, Test, Anticardiolipin Immunological   More FDA Info for this Device
510(K) Number	K013018
Device Name	System, Test, Anticardiolipin Immunological
Applicant	CORGENIX, INC. 12061 TEJON ST. WESTMINSTER, CO 80234 US Other 510(k) Applications for this Company
Contact	NANCI DEXTER 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	09/07/2001
Decision Date	09/20/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review