FDA 510(k) Application Details - K993109

Device Classification Name	Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls   More FDA Info for this Device
510(K) Number	K993109
Device Name	Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls
Applicant	PHARMACIA & UPJOHN CO. 5094 ST. ANDREWS DR. WESTERVILLLE, OH 43082 US Other 510(k) Applications for this Company
Contact	KAREN E MATIS Other 510(k) Applications for this Contact
Regulation Number	866.5100   More FDA Info for this Regulation Number
Classification Product Code	LJM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/17/1999
Decision Date	11/12/1999
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