FDA 510(k) Application Details - K983390

Device Classification Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)   More FDA Info for this Device
510(K) Number	K983390
Device Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
Applicant	COLUMBIA BIOSCIENCE, INC. 8775 M CENTRE PARK DR. #559 COLUMBIA, MD 21045 US Other 510(k) Applications for this Company
Contact	NORMAN JENKINS Other 510(k) Applications for this Contact
Regulation Number	866.5660   More FDA Info for this Regulation Number
Classification Product Code	MOB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/25/1998
Decision Date	11/18/1998
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