FDA 510(k) Application Details - K032203

Device Classification Name	System, Hemoglobin, Automated   More FDA Info for this Device
510(K) Number	K032203
Device Name	System, Hemoglobin, Automated
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	864.5620   More FDA Info for this Regulation Number
Classification Product Code	GKR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/18/2003
Decision Date	08/25/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review