FDA 510(k) Application Details - K954062

Device Classification Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)   More FDA Info for this Device
510(K) Number	K954062
Device Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
Applicant	SCIMEDX CORP. 400 FORD RD. DENVILLE, NJ 07834 US Other 510(k) Applications for this Company
Contact	THOMAS BRITTEN 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	08/29/1995
Decision Date	03/19/1996
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