FDA 510(k) Application Details - K020487

Device Classification Name	Nadh Oxidation/Nad Reduction, Alt/Sgpt   More FDA Info for this Device
510(K) Number	K020487
Device Name	Nadh Oxidation/Nad Reduction, Alt/Sgpt
Applicant	CARESIDE, INC. 6100 BRISTOL PKWY. CULVER CITY, CA 90230 US Other 510(k) Applications for this Company
Contact	KENNETH B ASARCH Other 510(k) Applications for this Contact
Regulation Number	862.1030   More FDA Info for this Regulation Number
Classification Product Code	CKA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/13/2002
Decision Date	06/04/2002
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