FDA 510(k) Applications Submitted by Sara Kastrup

FDA 510(k) Number	Submission Date	Device Name	Applicant
K143352	11/24/2014	IMMULITE 2000 Ferritin Calibration Verification Material, IMMULITE 2000 IGFBP-3 Calibration Verification Material	SIEMENS HEALTHCARE DIAGNOSTICS, INC.
K143504	12/10/2014	IMMULITE 2000 Albumin Calibration Verification Material, IMMULITE 2000 Myoglobin Calibration Verification Material	Siemens Healthcare Diagnostics Inc.