FDA 510(k) Application Details - K070199

Device Classification Name	Mixture, Hematology Quality Control   More FDA Info for this Device
510(K) Number	K070199
Device Name	Mixture, Hematology Quality Control
Applicant	Streck 7002 SOUTH 109TH ST. OMAHA, NE 68128 US Other 510(k) Applications for this Company
Contact	KERRIE OETTER Other 510(k) Applications for this Contact
Regulation Number	864.8625   More FDA Info for this Regulation Number
Classification Product Code	JPK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/22/2007
Decision Date	02/23/2007
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