FDA 510(k) Application Details - K082205

Device Classification Name	Test, Qualitative And Quantitative Factor Deficiency   More FDA Info for this Device
510(K) Number	K082205
Device Name	Test, Qualitative And Quantitative Factor Deficiency
Applicant	GENETIC TESTING INSTITUTE 20925 CROSSROADS CIRCLE SUITE 200 WAUKESHA, WI 53186-4054 US Other 510(k) Applications for this Company
Contact	MICHELLE A STAPLETON Other 510(k) Applications for this Contact
Regulation Number	864.7290   More FDA Info for this Regulation Number
Classification Product Code	GGP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/05/2008
Decision Date	11/20/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	HE - Hematology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review