FDA 510(k) Application Details - K082251

Device Classification Name	Albumin, Antigen, Antiserum, Control   More FDA Info for this Device
510(K) Number	K082251
Device Name	Albumin, Antigen, Antiserum, Control
Applicant	BECKMAN COULTER, INC. 200 SOUTH KRAEMER BLVD. MS 110 BREA, CA 92821 US Other 510(k) Applications for this Company
Contact	MARINE BOYAJIAN Other 510(k) Applications for this Contact
Regulation Number	866.5040   More FDA Info for this Regulation Number
Classification Product Code	DCF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/08/2008
Decision Date	04/08/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review