FDA 510(k) Application Details - K140790

Device Classification Name	Calibrator, Multi-Analyte Mixture   More FDA Info for this Device
510(K) Number	K140790
Device Name	Calibrator, Multi-Analyte Mixture
Applicant	SIEMENS HEALTHCARE DIAGNOSTICS 500 GBC DRIVE M/S 514 NEWARK, DE 19714 US Other 510(k) Applications for this Company
Contact	HELEN M LEE Other 510(k) Applications for this Contact
Regulation Number	862.1150   More FDA Info for this Regulation Number
Classification Product Code	JIX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/31/2014
Decision Date	06/15/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review