FDA 510(k) Applications Submitted by MARIA E TREJO

FDA 510(k) Number Submission Date Device Name Applicant
K060768 03/22/2006 PRECISION XTRA BLOOD B KETONE TEST STRIPS, OPTIUM BLOOD B KETONE TEST STRIPS ABBOTT DIABETES CARE INC.
K070984 04/06/2007 THE PRECISION / OPTIUM POINT OF CARE BLOOD GLUCOSE TEST STRIPS ABBOTT DIABETES CARE INC.


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