FDA 510(k) Application Details - K960392

Device Classification Name	Instrumentation, High Pressure Liquid Chromatography   More FDA Info for this Device
510(K) Number	K960392
Device Name	Instrumentation, High Pressure Liquid Chromatography
Applicant	BIO-RAD 4000 ALFRED NOBEL DR. HERCULES, CA 94547-1803 US Other 510(k) Applications for this Company
Contact	JOHN W NELSON Other 510(k) Applications for this Contact
Regulation Number	862.2260   More FDA Info for this Regulation Number
Classification Product Code	LDM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/1996
Decision Date	07/08/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review