FDA 510(k) Application Details - K955283

Device Classification Name	Abnormal Hemoglobin Quantitation   More FDA Info for this Device
510(K) Number	K955283
Device Name	Abnormal Hemoglobin Quantitation
Applicant	PRIMUS CORP. P.O. BOX 22599 KANSAS CITY, MO 64113 US Other 510(k) Applications for this Company
Contact	JIM NOFFSINGER Other 510(k) Applications for this Contact
Regulation Number	864.7415   More FDA Info for this Regulation Number
Classification Product Code	GKA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/16/1995
Decision Date	03/01/1996
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