FDA 510(k) Application Details - K120369

Device Classification Name	Hexokinase, Glucose   More FDA Info for this Device
510(K) Number	K120369
Device Name	Hexokinase, Glucose
Applicant	HITACHI CHEMICAL DIAGNOSTICS, INC. 630 CLYDE CT. MOUNTAIN VIEW, CA 94043 US Other 510(k) Applications for this Company
Contact	BUNICHIRO NAKAJIMA Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CFR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/06/2012
Decision Date	05/10/2012
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