FDA 510(k) Application Details - K020935

Device Classification Name	Glucose Oxidase, Glucose   More FDA Info for this Device
510(K) Number	K020935
Device Name	Glucose Oxidase, Glucose
Applicant	HEMOCUE, INC. 9229 CRANFORD DR. POTOMAC, MD 20854 US Other 510(k) Applications for this Company
Contact	R.J. SLOMOFF Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CGA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2002
Decision Date	04/03/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review