FDA 510(k) Application Details - K955278

Device Classification Name	Plasma, Coagulation Control   More FDA Info for this Device
510(K) Number	K955278
Device Name	Plasma, Coagulation Control
Applicant	BEHRING DIAGNOSTICS, INC. 151 UNIVERSITY AVE. WESTWOOD, MA 02090 US Other 510(k) Applications for this Company
Contact	KATHLEEN DRAY-LYONS Other 510(k) Applications for this Contact
Regulation Number	864.5425   More FDA Info for this Regulation Number
Classification Product Code	GGN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/17/1995
Decision Date	05/30/1996
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