FDA 510(k) Application Details - K983132

Device Classification Name	Igm, Antigen, Antiserum, Control   More FDA Info for this Device
510(K) Number	K983132
Device Name	Igm, Antigen, Antiserum, Control
Applicant	ABBOTT LABORATORIES 1920 HURD DR. IRVING, TX 75038 US Other 510(k) Applications for this Company
Contact	LINDA MORRIS Other 510(k) Applications for this Contact
Regulation Number	866.5550   More FDA Info for this Regulation Number
Classification Product Code	DFT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/08/1998
Decision Date	11/04/1998
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