FDA 510(k) Application Details - K130014

Device Classification Name	Assay, Glycosylated Hemoglobin   More FDA Info for this Device
510(K) Number	K130014
Device Name	Assay, Glycosylated Hemoglobin
Applicant	Sakae Corporation 575 Shirlynn Court Los Altos, CA 94022 US Other 510(k) Applications for this Company
Contact	ERICA B AMMIRATI Other 510(k) Applications for this Contact
Regulation Number	864.7470   More FDA Info for this Regulation Number
Classification Product Code	LCP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/02/2013
Decision Date	04/04/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review