FDA 510(k) Application Details - K050487

Device Classification Name	Lipoprotein, Low-Density, Antigen, Antiserum, Control   More FDA Info for this Device
510(K) Number	K050487
Device Name	Lipoprotein, Low-Density, Antigen, Antiserum, Control
Applicant	BIOKIT S.A. CAN MALE LLISSA D'AMUNT BARCELONA 08186 ES Other 510(k) Applications for this Company
Contact	JOAN GUIXER Other 510(k) Applications for this Contact
Regulation Number	866.5600   More FDA Info for this Regulation Number
Classification Product Code	DFC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/25/2005
Decision Date	04/26/2005
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