FDA 510(k) Application Details - K022528

Device Classification Name	Counter, Differential Cell   More FDA Info for this Device
510(K) Number	K022528
Device Name	Counter, Differential Cell
Applicant	IQ CORP. 11511 SW 127TH ST. MIAMI, FL 33176 US Other 510(k) Applications for this Company
Contact	H.G. HAINES Other 510(k) Applications for this Contact
Regulation Number	864.5220   More FDA Info for this Regulation Number
Classification Product Code	GKZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/2002
Decision Date	09/11/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review