FDA 510(k) Application Details - K964063

Device Classification Name	System, Test, Low Density, Lipoprotein   More FDA Info for this Device
510(K) Number	K964063
Device Name	System, Test, Low Density, Lipoprotein
Applicant	REFERENCE DIAGNOSTICS, INC. 23 CROSBY DR. BEDFORD, MA 01730 US Other 510(k) Applications for this Company
Contact	JOSEPH LAWLOR, PH.D. Other 510(k) Applications for this Contact
Regulation Number	862.1475   More FDA Info for this Regulation Number
Classification Product Code	MRR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/10/1996
Decision Date	11/20/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	Y
Expedited Review