FDA 510(k) Application Details - K071781

Device Classification Name	Platelet Factor 4 Radioimmunoassay   More FDA Info for this Device
510(K) Number	K071781
Device Name	Platelet Factor 4 Radioimmunoassay
Applicant	GENETIC TESTING INSTITUTE 20925 CROSSROADS CIRCLE SUITE 200 WAUKESHA, WI 53186-4054 US Other 510(k) Applications for this Company
Contact	SUZETTE C CHANCE Other 510(k) Applications for this Contact
Regulation Number	864.7695   More FDA Info for this Regulation Number
Classification Product Code	LCO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/02/2007
Decision Date	12/19/2007
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