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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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