FDA 510(k) Application Details - K020521

Device Classification Name	Multi-Analyte Controls, All Kinds (Assayed)   More FDA Info for this Device
510(K) Number	K020521
Device Name	Multi-Analyte Controls, All Kinds (Assayed)
Applicant	BECKMAN COULTER, INC. 200 SOUTH KRAEMER BLVD.,W-104 P.O. BOX 8000 BREA, CA 92822-8000 US Other 510(k) Applications for this Company
Contact	GAIL LEFEBVRE Other 510(k) Applications for this Contact
Regulation Number	862.1660   More FDA Info for this Regulation Number
Classification Product Code	JJY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/19/2002
Decision Date	03/01/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review