FDA 510(k) Application Details - K993294

Device Classification Name	Antinuclear Antibody, Antigen, Control   More FDA Info for this Device
510(K) Number	K993294
Device Name	Antinuclear Antibody, Antigen, Control
Applicant	DIAMEDIX CORP. 2140 NORTH MIAMI AVE. MIAMI, FL 33127 US Other 510(k) Applications for this Company
Contact	LYNNE STIRLING, PH.D Other 510(k) Applications for this Contact
Regulation Number	866.5100   More FDA Info for this Regulation Number
Classification Product Code	LKJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/01/1999
Decision Date	10/25/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review